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[ CAS No. 14161-84-3 ] {[proInfo.proName]}

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Chemical Structure| 14161-84-3
Chemical Structure| 14161-84-3
Structure of 14161-84-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 14161-84-3 ]

CAS No. :14161-84-3 MDL No. :MFCD03412454
Formula : C9H9ClO2 Boiling Point : -
Linear Structure Formula :- InChI Key :YRUBJDXEYFCYCX-UHFFFAOYSA-N
M.W : 184.62 Pubchem ID :13109535
Synonyms :

Calculated chemistry of [ 14161-84-3 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.8
TPSA : 37.3 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) : -5.72 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.72
Log Po/w (XLOGP3) : 2.41
Log Po/w (WLOGP) : 2.53
Log Po/w (MLOGP) : 2.55
Log Po/w (SILICOS-IT) : 2.35
Consensus Log Po/w : 2.31

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.74
Solubility : 0.335 mg/ml ; 0.00182 mol/l
Class : Soluble
Log S (Ali) : -2.84
Solubility : 0.27 mg/ml ; 0.00146 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.82
Solubility : 0.278 mg/ml ; 0.0015 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.75

Safety of [ 14161-84-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338-P310 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 14161-84-3 ]

* 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 [ 14161-84-3 ]
  • Downstream synthetic route of [ 14161-84-3 ]

[ 14161-84-3 ] Synthesis Path-Upstream   1~12

  • 1
  • [ 124-38-9 ]
  • [ 2039-85-2 ]
  • [ 14161-84-3 ]
Reference: [1] Journal of the American Chemical Society, 2008, vol. 130, # 45, p. 14936 - 14937
  • 2
  • [ 103040-42-2 ]
  • [ 14161-84-3 ]
Reference: [1] Journal of Organic Chemistry, 2003, vol. 68, # 19, p. 7234 - 7242
[2] Patent: US2014/187538, 2014, A1, . Location in patent: Page/Page column
  • 3
  • [ 201230-82-2 ]
  • [ 65130-47-4 ]
  • [ 14161-84-3 ]
Reference: [1] Journal of Organometallic Chemistry, 1982, vol. 232, # 1, p. 59 - 70
  • 4
  • [ 124-38-9 ]
  • [ 34887-78-0 ]
  • [ 14161-84-3 ]
Reference: [1] Angewandte Chemie, 1984, vol. 96, # 12, p. 978 - 979
  • 5
  • [ 1878-65-5 ]
  • [ 14161-84-3 ]
Reference: [1] Journal of Medicinal Chemistry, 1994, vol. 37, # 11, p. 1704 - 1711
[2] Patent: US2014/187538, 2014, A1,
  • 6
  • [ 1878-65-5 ]
  • [ 74-88-4 ]
  • [ 14161-84-3 ]
Reference: [1] Tetrahedron, 1997, vol. 53, # 38, p. 13149 - 13164
[2] Journal of the American Chemical Society, 2017, vol. 139, # 44, p. 15632 - 15635
  • 7
  • [ 53088-68-9 ]
  • [ 14161-84-3 ]
Reference: [1] Journal of Organic Chemistry, 2003, vol. 68, # 19, p. 7234 - 7242
[2] Patent: US2014/187538, 2014, A1,
  • 8
  • [ 41904-39-6 ]
  • [ 14161-84-3 ]
Reference: [1] Journal of Medicinal Chemistry, 1994, vol. 37, # 11, p. 1704 - 1711
  • 9
  • [ 14271-35-3 ]
  • [ 14161-84-3 ]
Reference: [1] Journal of Organic Chemistry, 1967, vol. 32, p. 3499 - 3506
  • 10
  • [ 1529-41-5 ]
  • [ 14161-84-3 ]
Reference: [1] Journal of Organic Chemistry, 1967, vol. 32, p. 3499 - 3506
  • 11
  • [ 82236-46-2 ]
  • [ 14161-84-3 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1983, vol. 31, # 3, p. 883 - 886
  • 12
  • [ 86998-06-3 ]
  • [ 14161-84-3 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1983, vol. 31, # 3, p. 883 - 886
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