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[ CAS No. 17609-47-1 ]

{[proInfo.proName]} (Synonyms:Ethyl L-valinate hydrochloride) ,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 17609-47-1
Chemical Structure| 17609-47-1
Structure of 17609-47-1 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 17609-47-1 ]

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Product Details of [ 17609-47-1 ]

CAS No. :17609-47-1 MDL No. :MFCD00012511
Formula : C7H16ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :PQGVTLQEKCJXKF-RGMNGODLSA-N
M.W :181.66 Pubchem ID :87181
Synonyms :
Ethyl L-valinate hydrochloride

Calculated chemistry of [ 17609-47-1 ]

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.86
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.72
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) : -6.17 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.74
Log Po/w (WLOGP) : 1.33
Log Po/w (MLOGP) : 1.08
Log Po/w (SILICOS-IT) : 0.4
Consensus Log Po/w : 0.91

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.8
Solubility : 2.89 mg/ml ; 0.0159 mol/l
Class : Very soluble
Log S (Ali) : -2.46
Solubility : 0.636 mg/ml ; 0.0035 mol/l
Class : Soluble
Log S (SILICOS-IT) : -0.85
Solubility : 25.6 mg/ml ; 0.141 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.93

Safety of [ 17609-47-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302+H312+H332-H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 17609-47-1 ]

* 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 [ 17609-47-1 ]
  • Downstream synthetic route of [ 17609-47-1 ]

[ 17609-47-1 ] Synthesis Path-Upstream   1~10

  • 1
  • [ 64-17-5 ]
  • [ 72-18-4 ]
  • [ 17609-47-1 ]
YieldReaction ConditionsOperation in experiment
6.1 kg at 0℃; for 18 h; Reflux; Large scale 5 kg (ie 42.7 mol) of L-valine and4kg anhydrous ethanol added to50L glass reactor, stirring to dissolve, cooling to 0 ~ 10 ,Slowly added dropwise 8.8L of thionyl chloride, dropping was completed, the reaction was warmed to reflux 18h,Concentrated to dry, at 15 ~ 20 ° C was added 15L isopropyl acetate beating 1h,Filtering with suction gave 6.1 kg of an off-white solid, intermediate 1, where R1 is ethyl.
Reference: [1] Tetrahedron, 2005, vol. 61, # 35, p. 8423 - 8442
[2] Journal of the Indian Chemical Society, 2001, vol. 78, # 3, p. 137 - 141
[3] Journal of the American Chemical Society, 2018, vol. 140, # 22, p. 6818 - 6822
[4] Chemistry of Natural Compounds, 1994, vol. 30, # 2, p. 238 - 244[5] Khimiya Prirodnykh Soedinenii, 1994, # 2, p. 261 - 268
[6] Tetrahedron, 1990, vol. 46, # 15, p. 5325 - 5332
[7] Helvetica Chimica Acta, 1995, vol. 78, p. 109 - 121
[8] Tetrahedron, 2007, vol. 63, # 14, p. 3031 - 3041
[9] European Journal of Medicinal Chemistry, 2011, vol. 46, # 1, p. 11 - 20
[10] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2011, vol. 50, # 9, p. 1157 - 1164
[11] Green Chemistry, 2012, vol. 14, # 5, p. 1350 - 1356
[12] Tetrahedron, 2012, vol. 68, # 49, p. 10218 - 10229,12
[13] Tetrahedron, 2012, vol. 68, # 49, p. 10218 - 10229
[14] Nucleosides, Nucleotides and Nucleic Acids, 2013, vol. 32, # 4, p. 161 - 173
[15] Journal of Heterocyclic Chemistry, 2013, vol. 50, # 5, p. 1067 - 1070
[16] Patent: CN107056720, 2017, A, . Location in patent: Paragraph 0058; 0059; 0060; 0061
[17] Journal of Medicinal Chemistry, 2018, vol. 61, # 7, p. 2707 - 2724
[18] European Journal of Organic Chemistry, 2018, vol. 2018, # 44, p. 6088 - 6091
  • 2
  • [ 72-18-4 ]
  • [ 17609-47-1 ]
Reference: [1] Liebigs Annalen der Chemie, 1985, # 9, p. 1917 - 1921
  • 3
  • [ 99474-03-0 ]
  • [ 17609-47-1 ]
Reference: [1] Liebigs Annalen der Chemie, 1985, # 9, p. 1917 - 1921
  • 4
  • [ 24601-74-9 ]
  • [ 17609-47-1 ]
Reference: [1] Liebigs Annalen der Chemie, 1985, # 9, p. 1917 - 1921
  • 5
  • [ 15136-26-2 ]
  • [ 17609-47-1 ]
Reference: [1] Liebigs Annalen der Chemie, 1985, # 9, p. 1917 - 1921
  • 6
  • [ 67436-18-4 ]
  • [ 17609-47-1 ]
Reference: [1] Synthesis, 2011, # 20, p. 3247 - 3254
  • 7
  • [ 427888-21-9 ]
  • [ 17609-47-1 ]
Reference: [1] Synthesis (Germany), 2016, vol. 48, # 13, p. 2036 - 2049
  • 8
  • [ 433735-03-6 ]
  • [ 17609-47-1 ]
Reference: [1] Synthesis (Germany), 2016, vol. 48, # 13, p. 2036 - 2049
  • 9
  • [ 99474-04-1 ]
  • [ 17609-47-1 ]
Reference: [1] Liebigs Annalen der Chemie, 1985, # 9, p. 1917 - 1921
  • 10
  • [ 99474-05-2 ]
  • [ 17609-47-1 ]
  • [ 99474-06-3 ]
Reference: [1] Liebigs Annalen der Chemie, 1985, # 9, p. 1917 - 1921
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