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[ CAS No. 827605-29-8 ] {[proInfo.proName]}

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Chemical Structure| 827605-29-8
Chemical Structure| 827605-29-8
Structure of 827605-29-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 827605-29-8 ]

CAS No. :827605-29-8 MDL No. :N/A
Formula : C11H14BClO2 Boiling Point : -
Linear Structure Formula :- InChI Key :OHPJVGZKIQIBRZ-UHFFFAOYSA-N
M.W : 224.49 Pubchem ID :16050224
Synonyms :

Calculated chemistry of [ 827605-29-8 ]

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.45
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 62.78
TPSA : 18.46 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.19 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 3.49
Log Po/w (WLOGP) : 2.11
Log Po/w (MLOGP) : 2.01
Log Po/w (SILICOS-IT) : 2.2
Consensus Log Po/w : 1.96

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.66
Solubility : 0.0491 mg/ml ; 0.000219 mol/l
Class : Soluble
Log S (Ali) : -3.56
Solubility : 0.0618 mg/ml ; 0.000275 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.14
Solubility : 0.0164 mg/ml ; 0.0000731 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.8

Safety of [ 827605-29-8 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 827605-29-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 827605-29-8 ]

[ 827605-29-8 ] Synthesis Path-Downstream   1~85

  • 1
  • [ 827605-29-8 ]
  • [ 36952-37-1 ]
  • [1-(4-Chloro-phenyl)-1-phenyl-meth-(Z)-ylidene]-(3-methyl-pyridin-2-yl)-amine [ No CAS ]
  • 2
  • [ 6944-25-8 ]
  • [ 126-30-7 ]
  • [ 827605-29-8 ]
  • 3
  • [ 827605-29-8 ]
  • [ 953813-12-2 ]
  • C16H21ClN2O [ No CAS ]
  • 4
  • [ 827605-29-8 ]
  • [ 953813-08-6 ]
  • C14H17ClN2 [ No CAS ]
  • 5
  • [ 827605-29-8 ]
  • [ 134-85-0 ]
  • 6
  • [ 67-56-1 ]
  • [ 10294-34-5 ]
  • [ 6944-25-8 ]
  • [ 126-30-7 ]
  • [ 827605-29-8 ]
  • 8
  • [ 1679-18-1 ]
  • [ 126-30-7 ]
  • [ 827605-29-8 ]
YieldReaction ConditionsOperation in experiment
87% In tetrahydrofuran; at 20℃; for 2.5h;Inert atmosphere; 4-Chlorophenylboronic acid (400 mg, 2.558 mmol) and 2,2-dimethyl-1,3-propanediol (293 mg, 2.814 mmol) were dissolved in THF (7 mL) and the mixture was stirred at rt for 2.5 h. The solvent was then removed in vacuo and the obtained beige solid was dissolved in CH2Cl2. The solution was washed with H2O, dried over Na2SO4 and the solvent was removed in vacuo to obtain para-chlorophenyl boronic acid neopentylglycol ester as a white solid (499 mg, 2.223 mmol, 87%). 1H NMR for this intermediate (DMSO-d6, 300 MHz) δ 7.71 (d, J = 8.3 Hz, 2H), 7.43 (d, J = 8.3 Hz, 2H), 3.77 (s, 4H), 0.97 (s, 6H).
In diethyl ether; at 20℃;Inert atmosphere; Molecular sieve; General procedure: To a Et2O solution of anorganoboronic acid (1.00 equiv) and 2,2-dimethylpropane-1,3-diol (neopentyl glycol)(1.02 equiv), 4A molecular sieves was added and the reaction mixture was stirred atroom temperature. After the reaction finished, the reaction mixture was filtered andconcentrated in vacuo. The residue was subjected to flash column chromatography(eluent: petroleum ether/ethyl acetate) or recrystallization to obtain the desired product
  • 9
  • [ 106-39-8 ]
  • [ 668987-38-0 ]
  • [ 827605-29-8 ]
  • 10
  • [ 827605-29-8 ]
  • [ 67-56-1 ]
  • [ 201230-82-2 ]
  • [ 1126-46-1 ]
  • [ 2050-68-2 ]
  • [ 90-98-2 ]
  • 11
  • [ 827605-29-8 ]
  • [ 201230-82-2 ]
  • [ 67-63-0 ]
  • [ 22913-11-7 ]
  • 12
  • [ 827605-29-8 ]
  • [ 201230-82-2 ]
  • [ 71-36-3 ]
  • [ 27942-64-9 ]
  • 13
  • [ 827605-29-8 ]
  • [ 1215180-93-0 ]
  • [ 1095091-93-2 ]
  • 14
  • [ 827605-29-8 ]
  • [ 1253579-22-4 ]
  • C33H23ClFNO2 [ No CAS ]
  • [ 1253579-36-0 ]
  • 15
  • [ 827605-29-8 ]
  • [ 68654-52-4 ]
  • [ 1261144-98-2 ]
  • 2,6-bis(4-chlorophenyl)-1-(pyridin-2-yl)piperidine [ No CAS ]
  • 2,6-bis(4-chlorophenyl)-1-(pyridin-2-yl)piperidine [ No CAS ]
  • 16
  • [ 827605-29-8 ]
  • [ 1466-76-8 ]
  • [ 938764-37-5 ]
  • 17
  • [ 827605-29-8 ]
  • [ 75748-09-3 ]
  • C22H30BClO4Si [ No CAS ]
  • 18
  • [ 827605-29-8 ]
  • [ 540-54-5 ]
  • [ 52944-34-0 ]
  • 19
  • [ 827605-29-8 ]
  • [ 71042-21-2 ]
  • [ 1308658-23-2 ]
  • 20
  • [ 827605-29-8 ]
  • [ 599-91-7 ]
  • [ 52944-34-0 ]
  • 21
  • [ 827605-29-8 ]
  • [ 1313442-28-2 ]
  • [ 1313442-43-1 ]
  • [ 1313442-51-1 ]
  • 22
  • [ 827605-29-8 ]
  • [ 273-53-0 ]
  • [ 1141-35-1 ]
  • 23
  • [ 827605-29-8 ]
  • diethyl 3-phenylprop-2-enyl phosphate [ No CAS ]
  • [ 949568-27-8 ]
  • 24
  • [ 827605-29-8 ]
  • diethyl 3-phenylprop-2-enyl phosphate [ No CAS ]
  • [ 1334512-13-8 ]
  • 25
  • [ 827605-29-8 ]
  • [ 768392-43-4 ]
  • (R)-3-(4-chlorophenyl)-3-phenyl-1-butene [ No CAS ]
  • [ 1334512-27-4 ]
  • 27
  • [ 827605-29-8 ]
  • [ 1354723-14-0 ]
  • [ 1354723-39-9 ]
  • 28
  • [ 827605-29-8 ]
  • [ 10375-59-4 ]
  • C6(11)CH5ClO2 [ No CAS ]
  • 29
  • [ 827605-29-8 ]
  • [ 52742-32-2 ]
  • [ 15429-21-7 ]
  • 30
  • [ 827605-29-8 ]
  • [ 92197-18-7 ]
  • [ 126086-73-5 ]
  • 31
  • [ 827605-29-8 ]
  • [ 1380288-25-4 ]
  • [ 119836-12-3 ]
  • 32
  • [ 827605-29-8 ]
  • [ 1372405-04-3 ]
  • [ 1380288-19-6 ]
  • 33
  • [ 827605-29-8 ]
  • [ 1372405-06-5 ]
  • [ 1380288-21-0 ]
  • 34
  • [ 827605-29-8 ]
  • [ 116-14-3 ]
  • [ 82907-01-5 ]
  • 35
  • [ 827605-29-8 ]
  • [ 1025506-03-9 ]
  • [ 1439838-58-0 ]
  • 36
  • [ 827605-29-8 ]
  • [ 591-51-5 ]
  • [ 124422-00-0 ]
YieldReaction ConditionsOperation in experiment
28% In diethyl ether; dibutyl ether; at -78℃;Inert atmosphere; General procedure: 4-Fluorophenylboronic acid neopentylglycol ester (187 mg, 0.9 mmol) was dissolved in dry Et2O (8 mL) and the solution cooled to -78 C. PhLi (1.8 M in n-Bu2O, 0.5 mL, 0.9 mmol) was then added slowly to the solution and the mixture was stirred at -78 C. The reaction was quenched after 30 min at -78 C with 5 mL 1 M aq HCl, and the biphasic mixture was stirred for 15 min at rt. The organic layer was then collected and the aqueous layer extracted with Et2O. All organic layers were combined, dried over Na2SO4 and concentrated in vacuo to obtain a yellow-orange viscous oil.
  • 37
  • [ 827605-29-8 ]
  • [ 264608-40-4 ]
  • 7-(4-chlorophenyl)-8-(pyridin-2-yl)-1,4-dioxa-8-azaspiro-[4.5]decane [ No CAS ]
  • 38
  • [ 637-87-6 ]
  • [ 201733-56-4 ]
  • [ 827605-29-8 ]
  • 39
  • [ 827605-29-8 ]
  • [ 1131-33-5 ]
  • [ 1536006-38-8 ]
  • 40
  • [ 827605-29-8 ]
  • [ 694-59-7 ]
  • [ 5969-83-5 ]
  • 41
  • [ 827605-29-8 ]
  • [ 73540-76-8 ]
  • [ 1415045-52-1 ]
  • 42
  • [ 827605-29-8 ]
  • [ 66-71-7 ]
  • copper (I) tert-butoxide [ No CAS ]
  • C18H12ClCuN2 [ No CAS ]
  • 43
  • [ 827605-29-8 ]
  • [ 110-82-7 ]
  • [ 829-32-3 ]
  • 44
  • [ 6944-25-8 ]
  • [ 827605-29-8 ]
  • 45
  • [ 4250-46-8 ]
  • [ 126-30-7 ]
  • [ 827605-29-8 ]
YieldReaction ConditionsOperation in experiment
In methanol; for 1h;Inert atmosphere; Schlenk technique; General procedure: All reactions were carried out under argon using standard Schlenk techniques. Boron trichloride (1.0 M solution in dichloromethane, 1.8 mL, for 1a-l) or boron tribromide (1.0 M solution in dichloromethane, 1.8 mL, for 1m-o) was added to a stirred solution of triarylstibane 1a-o (0.5 mmol) in dichloromethane (0.5 mL) at 0 C. The mixture was stirred for 2 h at 0 C (for 1a-l) or 4 h at room temperature (for 1m) or 24 h at room temperature (for 1n and 1o). The solvent was removed under reduced pressure at room temperature and the residual oil was dissolved in methanol (1.5 mL). After the mixture was stirred for 30 min, 2,2-dimethyl-1,3-propanediol (5.0 mmol) was added and the stirring was continued for 1 h. The solvent was removed under reduced pressure. The residue was purified on silica gel column chromatography (hexane: CH2Cl2) to give arylboronate 3. The products were confirmed by comparison of NMR data and MS spectra with that in the literature.
  • 47
  • [ 827605-29-8 ]
  • [ 404574-87-4 ]
  • C21H20ClNO [ No CAS ]
  • 48
  • [ 827605-29-8 ]
  • [ 870-50-8 ]
  • di-tert-butyl 1-(4-chlorophenyl)hydrazine-1,2-dicarboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
65% With water; copper diacetate; lithium tert-butoxide; In 1,2-dimethoxyethane; at 20℃;Inert atmosphere; General procedure: To a 10-mL, two-necked flask (flask A) were added Cu(OAc)2 (4.5 mg, 0.025 mmol) and LiOt-Bu (60.0 mg, 0.75 mmol), and the atmosphere inside the flask was replaced with N2 by flushing (3 ×). To the flask, DME (0.5 mL) and H2O (4.5 μL, 0.025 mmol) were added and the mixture was stirred for over 15 min. To another 10-mL two-necked flask (flask B), arylboronic ester 1 (0.25 mmol) and di-tert-butyl azodicarboxylate (2, 115.1 mg, 0.5 mmol) were added, and after flushing the atmosphere in the flask with N2 (3 ×), DME (0.5 mL) was added. The solution in flask B was added to flask A via syringe within 1 min. Flask B was rinsed with DME (0.2 mL) and the solution was added to the flask A. After stirring for 13.5-16 h at r.t., the reaction was diluted with EtOAc (4 mL) and H2O (2-3 mL) and quenched with 1 M citric acid to neutralize the system. The organic layer was evaporated under reduced pressure. The residue was purified by column chromatography (silica gel) to provide the hydrazine. Di-tert-butyl 1-(4-Chlorophenyl)hydrazine-1,2-dicarboxylate (3c) [14,15]. White solid; yield: 56.0 mg (65%); Rf = 0.31 (hexane-EtOAc, 5:1). 1H NMR (400 MHz, CDCl3): δ = 1.49 (s, 18 H), [6.64, 6.83 (br s, 1 H)], 7.26 (d, J = 6.0 Hz, 2 H), 7.36 (br, 2 H). 13C NMR (100 MHz, CDCl3): δ = 28.2, 28.3, 81.9, 82.8, 124.7, 128.6, 130.8, 140.8, 153.5, 155.5.
  • 49
  • [ 827605-29-8 ]
  • [ 17763-67-6 ]
  • [ 917-57-7 ]
  • [ 811830-11-2 ]
  • 50
  • [ 827605-29-8 ]
  • C22H23NO4 [ No CAS ]
  • C28H28ClNO4 [ No CAS ]
  • 51
  • [ 827605-29-8 ]
  • C22H22ClNO4 [ No CAS ]
  • C28H27Cl2NO4 [ No CAS ]
  • 52
  • [ 827605-29-8 ]
  • C23H25NO5 [ No CAS ]
  • C29H30ClNO5 [ No CAS ]
  • 53
  • [ 827605-29-8 ]
  • C22H16ClNO [ No CAS ]
  • 54
  • [ 827605-29-8 ]
  • [ 93501-08-7 ]
  • 55
  • [ 827605-29-8 ]
  • [ 13652-11-4 ]
  • [ 1010720-50-9 ]
  • 56
  • [ 827605-29-8 ]
  • [ 34143-82-3 ]
  • 4'-chloro-3-methyl-[1,1'-biphenyl]-2-carbaldehyde [ No CAS ]
  • 57
  • [ 827605-29-8 ]
  • [ 34143-82-3 ]
  • C20H16ClN [ No CAS ]
  • 58
  • [ 827605-29-8 ]
  • (S)-2-(naphthalen-2-yl)butan-2-yl acetate [ No CAS ]
  • (R)-2-(2-(4-chlorophenyl)butan-2-yl)naphthalene [ No CAS ]
  • 59
  • [ 827605-29-8 ]
  • [ 1071-46-1 ]
  • [ 14062-24-9 ]
  • 60
  • [ 827605-29-8 ]
  • methyl 3-(2-(benzyl(tert-butoxycarbonyl)amino)-4,6-dimethoxyphenyl)propiolate [ No CAS ]
  • 1-benzyl-4-(4-chlorophenyl)-5,6,7-trimethoxyquinolin-2(1H)-one [ No CAS ]
  • 61
  • [ 827605-29-8 ]
  • [ 64-17-5 ]
  • [ 93-89-0 ]
  • [ 2050-68-2 ]
  • [ 7335-27-5 ]
  • [ 106-48-9 ]
  • 62
  • [ 827605-29-8 ]
  • [ 2040-04-2 ]
  • 1-(4′-chloro-3-methoxy[1,1′-biphenyl]-2-yl)ethan-1-one [ No CAS ]
  • 63
  • [ 827605-29-8 ]
  • [ 42523-15-9 ]
  • 1-(4-chlorophenyl)-9H-fluoren-9-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
96% With carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II); at 150℃; for 2.5h;Microwave irradiation; Inert atmosphere; General procedure: A dried Biotage microwave vial equipped with a magnetic stirring bar and anitrogen inlet was sequentially charged with fluorenone (1) (0.5 mmol), boronic ester (6) (0.5 - 1mmol), pinacolone (0.5 mL) and RuH2(CO)(PPh3)3 (10 mol%). The reaction mixture was heatedunder MW irradiation at 150 C for 2.5 - 8 h. The reaction mixture was extracted with EtOAc (15mL), washed with brine, subjected to filtration, dried (Na2SO4) and concentrated under reducedpressure. Purification using flash column chromatography on silica gel (eluting with 1:9hexanes/ethyl acetate) afforded product (2).
  • 64
  • [ 827605-29-8 ]
  • [ 142-30-3 ]
  • 3-(4-chlorophenyl)-2,5-dimethylhexa-3,4-dien-2-ol [ No CAS ]
  • 65
  • [ 827605-29-8 ]
  • [ 556-96-7 ]
  • [ 104-46-1 ]
  • 1-(1-(4-chlorophenyl)-1-(4-methoxyphenyl)propan-2-yl)-3,5-dimethylbenzene [ No CAS ]
  • 66
  • [ 827605-29-8 ]
  • [ 930-22-3 ]
  • [ 20047-22-7 ]
YieldReaction ConditionsOperation in experiment
82% With N,N,N,N,-tetramethylethylenediamine; copper(l) chloride; lithium tert-butoxide; In N,N-dimethyl-formamide; at 60℃; for 10h;Sealed tube; Inert atmosphere; (1) Cuprous chloride (CuCl, 10 mol%), tetramethylethylenediamine (TMEDA, 15 mol%), tert-butanol under airLithium (LiOtBu, 2.5 eq), p-chloroaryl neopentyl glycol boron ester (2 eq) added to a sealed tube containing a magnetic tubeIn the tube, the reaction tube was flushed with argon three times. Under the protection of argon, 0.6 mL of N,N-dimethylformamide was added to the reaction tube.Add vinyl epoxy (0.25 mmol) to the reaction solution under argon, plug the piston, and place in a 60 C oil bath.Mix and react for 10 hours.(2) The material obtained in the step (1) is quenched by adding saturated ammonium chloride, and fully mixed with ethyl acetate, using short silicon.After the column has filtered off the solid residue, the organic phase is retained.(3) spinning the solvent in the organic phase obtained in the step (2) to obtain a crude product, which is then purified by a silica gel column.Things. The eluent was a mixture of petroleum ether and ethyl acetate with an isolated yield of 82% and a product purity of 100%.
  • 67
  • [ 827605-29-8 ]
  • [ 930-22-3 ]
  • [ 141-78-6 ]
  • C12H13ClO2 [ No CAS ]
  • 68
  • [ 827605-29-8 ]
  • [ 10075-72-6 ]
  • 1-(4-chlorophenyl)-8-(methylsulfanyl)naphthalene [ No CAS ]
  • 69
  • [ 827605-29-8 ]
  • [ 591-50-4 ]
  • N-(2,4-dimethoxybenzyl)but-3-enamide [ No CAS ]
  • 3-(4-chlorophenyl)-N-(2,4-dimethoxybenzyl)-4-phenylbutanamide [ No CAS ]
  • 70
  • [ 827605-29-8 ]
  • [ 230-27-3 ]
  • [ 1039045-16-3 ]
  • 71
  • [ 827605-29-8 ]
  • C16H15F3N2 [ No CAS ]
  • C20H13ClF3N [ No CAS ]
  • 72
  • [ 827605-29-8 ]
  • C16H15F3N2 [ No CAS ]
  • C14H8ClF3O [ No CAS ]
  • 73
  • [ 827605-29-8 ]
  • [ 10228-77-0 ]
  • N-((4’-chloro-3-methyl-[1,1’-biphenyl]-2-yl)methyl)aniline [ No CAS ]
  • 74
  • [ 827605-29-8 ]
  • [ 5765-65-1 ]
  • [ 1619992-39-0 ]
  • 4-((1S*,2S*)-2-(4-chlorophenyl)spiro[2.11]tetradecan-1-yl)morpholine [ No CAS ]
  • 75
  • [ 827605-29-8 ]
  • [ 5765-65-1 ]
  • [ 65051-83-4 ]
  • 4-((1S*,2R*,3S*)-3-(4-chlorophenyl)-2-methyl-2-phenylcyclopropyl)morpholine [ No CAS ]
  • 4-(3-(4-chlorophenyl)-2-methyl-2-phenylcyclopropyl)morpholine [ No CAS ]
  • 76
  • [ 827605-29-8 ]
  • [ 29786-93-4 ]
  • C15H23BClO2(1-)*Li(1+) [ No CAS ]
  • 77
  • [ 827605-29-8 ]
  • [ 407-16-9 ]
  • 78
  • [ 827605-29-8 ]
  • [ 798553-21-6 ]
  • 4'-chloro-[1,1'-biphenyl]-4-yl trifluoromethanesulfonate [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With dichloro(N-(diphenylphosphino)-N-isopropyl-1,1-diphenylphosphinamine) digold(I); [bis(acetoxy)iodo]benzene; silver(I) 4-methylbenzenesulfonate; In 1,1,2-trichloroethane; at 110℃; for 1h;Schlenk technique; Inert atmosphere; General procedure: To a dried Schlenk tube was added 1f (8.9 mg, 0.01 mmol), AgOTs (11.2 mg, 0.04mmol), PhI(OAc)2 (84.0 mg, 0.26 mmol) and anhydrous TCE (1,1,2-trichloroethane, 1mL) at room temperature under an argon atmosphere. After vigorously stirring for 30min at room temperature, 2 (0.20 mmol) and 3 (0.26 mmol) in 1 mL anhydrous TCEwas added under an argon atmosphere, and then the reaction mixture was stirred at 110oC for 1-2 h. The reaction mixture was concentrated under reduced pressure and theresulting residue was purified by flash chromatography on silica gel (petroleumether/ethyl acetate) to give desired coupling product 4.
  • 79
  • [ 827605-29-8 ]
  • [ 579-74-8 ]
  • 1-(4′-chloro-3-methoxy[1,1′-biphenyl]-2-yl)ethan-1-one [ No CAS ]
  • 80
  • [ 827605-29-8 ]
  • [ 98-86-2 ]
  • [ 893739-17-8 ]
  • 1-(4,4′′-dichloro[1,1′:3′,1′′-terphenyl]-2′-yl)ethan-1-one [ No CAS ]
  • 81
  • [ 456-21-3 ]
  • [ 201733-56-4 ]
  • [ 827605-29-8 ]
  • 82
  • [ 827605-29-8 ]
  • [ 1221640-33-0 ]
  • [ 201230-82-2 ]
  • [ 1173294-91-1 ]
  • 83
  • [ 827605-29-8 ]
  • (2-allylphenyl)(naphthalen-2-yl)methyl tert-butyl carbonate [ No CAS ]
  • 2-((1R*,2R*)-2-(4-chlorobenzyl)-2,3-dihydro-1H-inden-1-yl)naphthalene [ No CAS ]
  • 84
  • [ 827605-29-8 ]
  • C26H28O4 [ No CAS ]
  • 2-((1R,2R)-2-(4-chlorobenzyl)-2,3-dihydro-1H-inden-1-yl)-6-methoxynaphthalene [ No CAS ]
  • 85
  • [ 827605-29-8 ]
  • C15H24O [ No CAS ]
  • C21H27ClO [ No CAS ]
  • C21H27ClO [ No CAS ]
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