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[ CAS No. 80945-86-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 80945-86-4
Chemical Structure| 80945-86-4
Structure of 80945-86-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 80945-86-4 ]

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Product Details of [ 80945-86-4 ]

CAS No. :80945-86-4 MDL No. :MFCD04971822
Formula : C7H3BrClNS Boiling Point : No data available
Linear Structure Formula :- InChI Key :IJQSMNIZBBEBKI-UHFFFAOYSA-N
M.W : 248.53 Pubchem ID :2049871
Synonyms :

Calculated chemistry of [ 80945-86-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 52.33
TPSA : 41.13 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.0 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.54
Log Po/w (XLOGP3) : 3.96
Log Po/w (WLOGP) : 3.71
Log Po/w (MLOGP) : 2.84
Log Po/w (SILICOS-IT) : 4.46
Consensus Log Po/w : 3.5

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.48
Solubility : 0.00821 mg/ml ; 0.000033 mol/l
Class : Moderately soluble
Log S (Ali) : -4.52
Solubility : 0.00743 mg/ml ; 0.0000299 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -4.44
Solubility : 0.00896 mg/ml ; 0.0000361 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.36

Safety of [ 80945-86-4 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H317-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 80945-86-4 ]

* 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.

  • Downstream synthetic route of [ 80945-86-4 ]

[ 80945-86-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 51618-30-5 ]
  • [ 80945-86-4 ]
YieldReaction ConditionsOperation in experiment
96% General procedure: A mixture of the 2-mercaptobenzo[d]thiazole (>1 g, 1 equiv) and sul-furyl chloride (10 equiv) was stirred at 20-25 C for 15 min. Next, H 2 O(2 equiv) was added and the mixture was stirred at 20-25 C for anadditional 3 h. A sample was taken, quenched with MeCN/H 2 O (2:1)and analyzed by HPLC. After completion of the reaction, the mixturewas diluted with MeCN (5 volumes) and slowly quenched with H 2 O(20 volumes). The product precipitated from the aqueous solution.The solid was collected and washed with H 2 O. Drying under vacuumafforded the pure product. In the case of the liquid product 2-chloro-benzo[d]thiazole (13), the reaction mixture was extracted withEtOAc. The organic layer was then dried and concentrated to affordthe product as an oil.
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