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[ CAS No. 90891-21-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 90891-21-7
Chemical Structure| 90891-21-7
Structure of 90891-21-7 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 90891-21-7 ]

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Product Details of [ 90891-21-7 ]

CAS No. :90891-21-7 MDL No. :MFCD00190691
Formula : C12H18ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :PTFKZMFFSIYCOV-MERQFXBCSA-N
M.W : 243.73 Pubchem ID :2734606
Synonyms :
Chemical Name :H-HoPhe-OEt.HCl

Calculated chemistry of [ 90891-21-7 ]

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.42
Num. rotatable bonds : 6
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 66.4
TPSA : 52.32 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) : -5.96 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.57
Log Po/w (WLOGP) : 2.31
Log Po/w (MLOGP) : 2.25
Log Po/w (SILICOS-IT) : 2.12
Consensus Log Po/w : 1.85

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.85
Solubility : 0.343 mg/ml ; 0.00141 mol/l
Class : Soluble
Log S (Ali) : -3.32
Solubility : 0.118 mg/ml ; 0.000482 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.38
Solubility : 0.101 mg/ml ; 0.000413 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.16

Safety of [ 90891-21-7 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 90891-21-7 ]

* 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 [ 90891-21-7 ]
  • Downstream synthetic route of [ 90891-21-7 ]

[ 90891-21-7 ] Synthesis Path-Upstream   1~10

  • 1
  • [ 90891-21-7 ]
  • [ 89396-94-1 ]
Reference: [1] Journal of Medicinal Chemistry, 1989, vol. 32, # 2, p. 289 - 297
[2] Journal of Medicinal Chemistry, 1989, vol. 32, # 2, p. 289 - 297
  • 2
  • [ 64-17-5 ]
  • [ 943-73-7 ]
  • [ 90891-21-7 ]
Reference: [1] Journal of Medicinal Chemistry, 1985, vol. 28, # 11, p. 1596 - 1602
[2] Synthesis, 2001, # 7, p. 1007 - 1009
[3] Journal of Medicinal Chemistry, 1989, vol. 32, # 2, p. 289 - 297
  • 3
  • [ 943-73-7 ]
  • [ 90891-21-7 ]
Reference: [1] Patent: US4439364, 1984, A,
  • 4
  • [ 115276-75-0 ]
  • [ 536-74-3 ]
  • [ 90891-21-7 ]
Reference: [1] Advanced Synthesis and Catalysis, 2007, vol. 349, # 14-15, p. 2375 - 2379
  • 5
  • [ 16503-46-1 ]
  • [ 90891-21-7 ]
Reference: [1] Journal of Medicinal Chemistry, 1989, vol. 32, # 2, p. 289 - 297
  • 6
  • [ 1012-05-1 ]
  • [ 90891-21-7 ]
Reference: [1] Journal of Medicinal Chemistry, 1989, vol. 32, # 2, p. 289 - 297
  • 7
  • [ 5440-40-4 ]
  • [ 90891-21-7 ]
Reference: [1] Journal of Medicinal Chemistry, 1989, vol. 32, # 2, p. 289 - 297
  • 8
  • [ 46460-23-5 ]
  • [ 90891-21-7 ]
Reference: [1] Organic Letters, 2008, vol. 10, # 10, p. 2031 - 2034
  • 9
  • [ 90315-82-5 ]
  • [ 90891-21-7 ]
Reference: [1] Green Chemistry, 2018, vol. 20, # 19, p. 4418 - 4422
  • 10
  • [ 129277-08-3 ]
  • [ 90891-21-7 ]
Reference: [1] Green Chemistry, 2018, vol. 20, # 19, p. 4418 - 4422
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