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[ CAS No. 58101-60-3 ] {[proInfo.proName]}

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Excepted Quantity USD 0.00
Limited Quantity USD 15-60
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Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 58101-60-3
Chemical Structure| 58101-60-3
Structure of 58101-60-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 58101-60-3 ]

CAS No. :58101-60-3 MDL No. :MFCD04038661
Formula : C7H10O2 Boiling Point : -
Linear Structure Formula :- InChI Key :CEOILRYKIJRPBZ-UHFFFAOYSA-N
M.W : 126.15 Pubchem ID :1514118
Synonyms :

Calculated chemistry of [ 58101-60-3 ]

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.57
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 34.46
TPSA : 26.3 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.19 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.03
Log Po/w (XLOGP3) : 1.24
Log Po/w (WLOGP) : 1.13
Log Po/w (MLOGP) : 1.13
Log Po/w (SILICOS-IT) : 1.1
Consensus Log Po/w : 1.32

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.27
Solubility : 6.75 mg/ml ; 0.0535 mol/l
Class : Very soluble
Log S (Ali) : -1.39
Solubility : 5.14 mg/ml ; 0.0407 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.6
Solubility : 31.4 mg/ml ; 0.249 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.68

Safety of [ 58101-60-3 ]

Signal Word:Danger Class:3,8
Precautionary Statements:P280-P305+P351+P338 UN#:2924
Hazard Statements:H225-H315-H318 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 58101-60-3 ]

* 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.

  • Upstream synthesis route of [ 58101-60-3 ]
  • Downstream synthetic route of [ 58101-60-3 ]

[ 58101-60-3 ] Synthesis Path-Upstream   1~16

  • 1
  • [ 67-56-1 ]
  • [ 201230-82-2 ]
  • [ 142-29-0 ]
  • [ 4630-80-2 ]
  • [ 2258-56-2 ]
  • [ 39590-04-0 ]
  • [ 58101-60-3 ]
Reference: [1] Journal of Organic Chemistry, 2002, vol. 67, # 14, p. 5005 - 5008
  • 2
  • [ 67-56-1 ]
  • [ 7686-77-3 ]
  • [ 58101-60-3 ]
YieldReaction ConditionsOperation in experiment
99%
Stage #1: With 1,1'-carbonyldiimidazole In dichloromethane at 0 - 20℃; for 4 h;
To a solution of 1.1 (10 g, 89 mmol) in DCM (100 mL) at 0° C. under N2 atmosphere was added 1,1-carbonyldiimidazole (43 g, 267 mmol). The mixture was stirred at room temperature for 4 hours, then MeOH (100 mL) was added. The mixture was allowed to stir overnight. The solvent was evaporated at low temperature to afford 2 (11.2 g, 99percent).
Reference: [1] Patent: US2007/254952, 2007, A1, . Location in patent: Page/Page column 35
[2] Nucleosides, Nucleotides and Nucleic Acids, 2001, vol. 20, # 4-7, p. 661 - 664
[3] ChemMedChem, 2011, vol. 6, # 9, p. 1559 - 1565
[4] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 19, p. 5336 - 5339
  • 3
  • [ 7686-77-3 ]
  • [ 74-88-4 ]
  • [ 58101-60-3 ]
YieldReaction ConditionsOperation in experiment
96% With potassium carbonate In DMF (N,N-dimethyl-formamide) at 20℃; for 16 h; To a solution of 3-cyclopentene-1-carboxylic acid (Org. Synth. 75, PL95-200, 1998) (31.5 g, 281 mmol) in anhydrous N, N-DIMETHYLFORMAMIDE (300 mL), under an atmosphere of nitrogen, was added potassium carbonate (97 g, 703 mmol), and iodomethane (35 mL, 563 mmol). The resulting mixture was stirred at room temperature for 16 hours, then poured into water (1 litre), and extracted with diethyl ether (3 x 400 mL). The combined diethyl ether layers were washed with water (3 x 500 mL), saturated NACL (200 mL), dried over MGS04, filtered and concentrated I71 VACUO, to give 34 g (96 percent) of crude product. H NMR (CDC13, 500 MHz) : 8 5.64 (s, 2H), 3.68 (s, 3H), 3.11 (quintet, J = 8.5 Hz, 1H), 2.63 (d, J = 8.3 Hz, 4 H).
96% With potassium carbonate In DMF (N,N-dimethyl-formamide) at 20℃; for 16 h; To a solution of 3-CYCLOPENTENE-1-CARBOXYLIC acid (Org. Synth. 75, PL95-200, 1998) (31.5 g, 281 mmol) in anhydrous N, N-DIMETHYLFORMAMIDE (300 mL), under an atmosphere of nitrogen, was added potassium carbonate (97 g, 710 MMOL), and iodomethane (35 mL, 560 mmol). The resulting mixture was stirred at room temperature for 16 h, then poured into water (1 L), and extracted with diethyl ether (3 x 400 mL). The combined diethyl ether layers were washed with water (3 x 500 mL), saturated NACI (200 ML), dried over MGS04, filtered and concentrated in vacuo, to give 34 g (96 percent). 'H NMR (CDCL3, 500 MHz) : 8 5.64 (s, 2H), 3.68 (s, 3H), 3.11 (quintet, J = 8.5 Hz, 1H), 2.63 (d, J = 8.3 Hz, 4 H).
96% With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 16 h; INTERMEDIATE 21; Step A; To a solution of 3-cyclopentene-1-carboxylic acid (Org. Synth. 75, p195-200, 1998) (31.5 g, 281 mmol) in anhydrous N,N-dimethylformamide (300 mL), under an atmosphere of nitrogen, was added potassium carbonate (97 g, 710 mmol), and iodomethane (35 mL, 560 mmol). The resulting mixture was stirred at room temperature for 16 h, then poured into water (1 L), and extracted with diethyl ether (3.x.400 mL). The combined diethyl ether layers were washed with water (3.x.500 mL), saturated NaCl (200 mL), dried over MgSO4, filtered and concentrated in vacuo, to give 34 g (96percent).1H NMR (CDCl3, 500 MHz): δ 5.64 (s, 2H), 3.68 (s, 3H), 3.11 (quintet, J=8.5 Hz, 1H), 2.63 (d, J=8.3 Hz, 4H).
Reference: [1] Patent: WO2004/41777, 2004, A2, . Location in patent: Page 41-42
[2] Patent: WO2004/94371, 2004, A2, . Location in patent: Page 81-82
[3] Patent: US2008/81803, 2008, A1, . Location in patent: Page/Page column 35
[4] Chemical Communications, 2013, vol. 49, # 100, p. 11758 - 11760
  • 4
  • [ 84646-68-4 ]
  • [ 58101-60-3 ]
Reference: [1] Organic Syntheses, 1998, vol. 75, p. 195 - 195
[2] Synlett, 2005, # 5, p. 765 - 768
[3] Patent: EP339669, 1989, A1,
[4] ChemMedChem, 2011, vol. 6, # 9, p. 1559 - 1565
  • 5
  • [ 54385-33-0 ]
  • [ 58101-60-3 ]
Reference: [1] Russian Chemical Bulletin, 1994, vol. 43, # 8, p. 1425 - 1426[2] Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1994, # 8, p. 1503 - 1504
  • 6
  • [ 84646-68-4 ]
  • [ 58101-60-3 ]
Reference: [1] Patent: EP339669, 1989, A1,
  • 7
  • [ 67-56-1 ]
  • [ 201230-82-2 ]
  • [ 142-29-0 ]
  • [ 4630-80-2 ]
  • [ 2258-56-2 ]
  • [ 39590-04-0 ]
  • [ 58101-60-3 ]
Reference: [1] Journal of Organic Chemistry, 2002, vol. 67, # 14, p. 5005 - 5008
  • 8
  • [ 67-56-1 ]
  • [ 3744-80-7 ]
  • [ 58101-60-3 ]
Reference: [1] Journal of Organic Chemistry, 1983, vol. 48, # 20, p. 3594 - 3597
[2] Synthetic Communications, 1992, vol. 22, # 22, p. 3197 - 3204
  • 9
  • [ 35357-77-8 ]
  • [ 58101-60-3 ]
Reference: [1] Synlett, 2005, # 5, p. 765 - 768
  • 10
  • [ 67-56-1 ]
  • [ 58101-60-3 ]
Reference: [1] European Journal of Organic Chemistry, 2009, # 25, p. 4273 - 4283
  • 11
  • [ 7686-77-3 ]
  • [ 58101-60-3 ]
Reference: [1] Synthetic Communications, 1992, vol. 22, # 22, p. 3197 - 3204
  • 12
  • [ 67-56-1 ]
  • [ 58101-60-3 ]
Reference: [1] European Journal of Organic Chemistry, 2008, # 26, p. 4412 - 4415
  • 13
  • [ 1587-26-4 ]
  • [ 108-59-8 ]
  • [ 58101-60-3 ]
Reference: [1] Tetrahedron Letters, 1985, vol. 26, # 27, p. 3267 - 3270
  • 14
  • [ 88326-51-6 ]
  • [ 58101-60-3 ]
Reference: [1] ChemMedChem, 2011, vol. 6, # 9, p. 1559 - 1565
  • 15
  • [ 67-56-1 ]
  • [ 58191-35-8 ]
  • [ 58101-60-3 ]
Reference: [1] Journal of Organic Chemistry, 1976, vol. 41, p. 1421 - 1425
  • 16
  • [ 58101-60-3 ]
  • [ 25125-21-7 ]
YieldReaction ConditionsOperation in experiment
100% With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 18 h; To a solution of 2 (8.6 g, 68 mmol) in THF (40.0 mL) at 0° C. was added LAH (54 mL, 1M solution in THF) under N2 atmosphere. The mixture was stirred at ambient temperature for 18 hours. The reaction mixture was quenched with water and NaOH (10 w/t percent). The mixture was filtered through celite and solvent was removed to give compound 3 (6.6 g, 100percent).
95% With lithium aluminium tetrahydride In diethyl ether at 0 - 20℃; Inert atmosphere To a suspension of lithium aluminum hydride (15.2g, 0.40 mol) in anhydrous ether (1 L) at 0°C under nitrogen, was added the solution of methyl cyclopent-3-enecarboxylate (50 g, 0.40 mol) in ether (300 mL) dropwise over 5 hrs. The suspension was stirred at room temperature overnight. TLC indicated the completion of the reaction. The reaction was re-cooled to 0°C. Saturated solution of Na2S04 (32 mL) was added dropwise to quench the reaction. After the addition was complete, the mixture was stirred for another 3 hrs and was filtered through a pad of celite. Evaporation of solvent afforded cyclopent-3-enylmethanol 146-2 (37.3 g, 95 percent) as a colorless liquid.
Reference: [1] Patent: US2007/254952, 2007, A1, . Location in patent: Page/Page column 35
[2] Tetrahedron Asymmetry, 1994, vol. 5, # 9, p. 1649 - 1652
[3] Patent: WO2017/177326, 2017, A1, . Location in patent: Page/Page column 93; 94
[4] Synlett, 2005, # 5, p. 765 - 768
[5] Tetrahedron Asymmetry, 2013, vol. 24, # 8, p. 449 - 456
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