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[ CAS No. 81765-97-1 ] {[proInfo.proName]}

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Chemical Structure| 81765-97-1
Chemical Structure| 81765-97-1
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Product Details of [ 81765-97-1 ]

CAS No. :81765-97-1 MDL No. :MFCD00458475
Formula : C11H11ClN2S Boiling Point : -
Linear Structure Formula :- InChI Key :VBBUCJFANWYVMU-UHFFFAOYSA-N
M.W : 238.74 Pubchem ID :290237
Synonyms :

Calculated chemistry of [ 81765-97-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.45
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 64.82
TPSA : 54.02 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.82 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.88
Log Po/w (XLOGP3) : 4.14
Log Po/w (WLOGP) : 3.53
Log Po/w (MLOGP) : 2.78
Log Po/w (SILICOS-IT) : 5.05
Consensus Log Po/w : 3.68

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.37
Solubility : 0.0101 mg/ml ; 0.0000424 mol/l
Class : Moderately soluble
Log S (Ali) : -4.98
Solubility : 0.00249 mg/ml ; 0.0000104 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.72
Solubility : 0.00459 mg/ml ; 0.0000192 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.77

Safety of [ 81765-97-1 ]

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 [ 81765-97-1 ]

* 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 [ 81765-97-1 ]
  • Downstream synthetic route of [ 81765-97-1 ]

[ 81765-97-1 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 19819-15-9 ]
  • [ 81765-97-1 ]
YieldReaction ConditionsOperation in experiment
71% Reflux General procedure: The different thieno[2,3-d]pyrimidin-4-one (6a-d or f-i) (1 eq.) and phosphoryl chloride (2.9 mL/mmoleq.) were refluxed for 8 h. The reaction mixture was then cooled in an ice-bath and carefully neutralised by the addition of aqueous saturated NaHCO3 solution. The resulting mixture was extracted with ethylacetate (15 mL/mmol eq.), the organic layer was separated, dried over MgSO4 and concentrated. The crude residue was purified by flash column chromatography eluting with n-hexane-EtOAc 100:0 v/vincreasing to n-hexane-EtOAc 85:15 v/v unless otherwise stated.
Reference: [1] Chemical & Pharmaceutical Bulletin, 1982, vol. 30, # 1, p. 326 - 332
[2] European Journal of Medicinal Chemistry, 2016, vol. 123, p. 31 - 47
[3] Synthesis, 2001, # 14, p. 2119 - 2123
  • 2
  • [ 4506-71-2 ]
  • [ 81765-97-1 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 2007, vol. 55, # 5, p. 776 - 779
[2] Synthesis, 2001, # 14, p. 2119 - 2123
[3] Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1982, vol. <B> 21, # 7, p. 666 - 668
[4] European Journal of Medicinal Chemistry, 2016, vol. 123, p. 31 - 47
  • 3
  • [ 19819-15-9 ]
  • [ 81765-97-1 ]
Reference: [1] Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1982, vol. <B> 21, # 7, p. 666 - 668
[2] Chemical and Pharmaceutical Bulletin, 2007, vol. 55, # 5, p. 776 - 779
  • 4
  • [ 108-94-1 ]
  • [ 81765-97-1 ]
Reference: [1] European Journal of Medicinal Chemistry, 2016, vol. 123, p. 31 - 47
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