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[ CAS No. 4089-07-0 ] {[proInfo.proName]}

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Chemical Structure| 4089-07-0
Chemical Structure| 4089-07-0
Structure of 4089-07-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 4089-07-0 ]

CAS No. :4089-07-0 MDL No. :MFCD00063047
Formula : C11H16ClNO3 Boiling Point : -
Linear Structure Formula :- InChI Key :BQULAXAVRFIAHN-PPHPATTJSA-N
M.W : 245.70 Pubchem ID :2724939
Synonyms :

Calculated chemistry of [ 4089-07-0 ]

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 5
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 63.62
TPSA : 72.55 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) : -6.72 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.52
Log Po/w (WLOGP) : 1.63
Log Po/w (MLOGP) : 1.39
Log Po/w (SILICOS-IT) : 1.28
Consensus Log Po/w : 1.16

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.27
Solubility : 1.32 mg/ml ; 0.00539 mol/l
Class : Soluble
Log S (Ali) : -2.65
Solubility : 0.547 mg/ml ; 0.00223 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.4
Solubility : 0.969 mg/ml ; 0.00394 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.06

Safety of [ 4089-07-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 4089-07-0 ]

* 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 [ 4089-07-0 ]
  • Downstream synthetic route of [ 4089-07-0 ]

[ 4089-07-0 ] Synthesis Path-Upstream   1~6

  • 1
  • [ 4089-07-0 ]
  • [ 658-79-7 ]
Reference: [1] Chemische Berichte, 1960, vol. 93, p. 2387 - 2394
  • 2
  • [ 4089-07-0 ]
  • [ 72594-77-5 ]
YieldReaction ConditionsOperation in experiment
84% With triethylamine In dichloromethane at 38 - 40℃; General procedure: L-Phenylalanine methyl ester hydrochloride (5.0 g, 23.2 mmol), triethyl amine (2.47 g, 24.4 mmol) and 2 (7.24 g, 24.4 mmol) were added to dichloromethane (50 mL) and stirred at reflux temp (38-40°C) for 5h. After completion of the reaction, filtered to remove salts and the filtrate was washed with 5percent KHSO4 (20 mL), water (25 mL), brine (25 mL), and dried over sodium sulfate. The solvent was evaporated under reduced pressure to obtain a pale yellow oil. The oil was purified by column chromatography (silica gel, ethyl acetate/ hexane, 8:2) to afford 5.96 g (92percent) Methyl (tert-butoxycarbonyl)-L-phenylalaninate as a colorless oil.
Reference: [1] Synthetic Communications, 2017, vol. 47, # 22, p. 2127 - 2132
  • 3
  • [ 24424-99-5 ]
  • [ 4089-07-0 ]
  • [ 72594-77-5 ]
Reference: [1] Patent: US2003/176498, 2003, A1,
  • 4
  • [ 4089-07-0 ]
  • [ 17083-23-7 ]
Reference: [1] Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1982, vol. 37, # 12, p. 1652 - 1658
  • 5
  • [ 64-17-5 ]
  • [ 60-18-4 ]
  • [ 4089-07-0 ]
Reference: [1] Helvetica Chimica Acta, 1995, vol. 78, p. 109 - 121
[2] Journal of the American Chemical Society, 2001, vol. 123, # 31, p. 7534 - 7538
[3] Green Chemistry, 2016, vol. 18, # 16, p. 4374 - 4392
[4] International Journal of Pharmaceutics, 2018, vol. 546, # 1-2, p. 31 - 38
  • 6
  • [ 1634-04-4 ]
  • [ 60-18-4 ]
  • [ 4089-07-0 ]
Reference: [1] Patent: US5506244, 1996, A,
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