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87566-39-0

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87566-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87566-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,6 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87566-39:
(7*8)+(6*7)+(5*5)+(4*6)+(3*6)+(2*3)+(1*9)=180
180 % 10 = 0
So 87566-39-0 is a valid CAS Registry Number.

87566-39-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(furan-2-yl)-3,9-dimethyl-2,4,4a,5-tetrahydro-1H-pyrazino[1,2-a][1,4]benzodiazepine

1.2 Other means of identification

Product number -
Other names Pyrazino(1,2-a)(1,4)benzodiazepine,1,2,3,4,4a,5-hexahydro-3,9-dimethyl-7-(2-furanyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:87566-39-0 SDS

87566-39-0Downstream Products

87566-39-0Relevant articles and documents

[1,2]-Fused 1,4-benzodiazepine compounds, process for their preparation and compositions containing them

-

, (2008/06/13)

[1,2]-fused 1,4-benzodiazepine compounds are disclosed corresponding to the general formula I STR1 wherein X is an oxygen or sulfur atom or an optionally substituted imino group, R1 is a hydrogen or halogen atom, lower alkyl radical, a lower alkoxy radical or a nitro group and R2 is a hydrogen or halogen atom, a lower alkyl radical, a lower alkoxy radical or a nitro group, or if R1 is a hydrogen atom, R2 may also be a lower alkylthio radical, or, if R1 is a hydrogen atom and X is a sulfur atom or an imino group, R2 may be a trifluoromethyl radical; or R1 and R2 are bonded to adjacent carbon atoms and together denote a methylenedioxy or ethylenedioxy radical; R3 is an optionally substituted furyl, thienyl, pyrrolyl or pyridyl radical and n is zero or, if R3 is furyl or thienyl, n may be 0 or 1. The compounds may be in the form of their optical isomers or acid addition salts. The compounds exhibit neuroleptic properties. Processes for preparing the compounds and pharmaceutical compositions containing them are also disclosed.

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