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59467-68-4

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59467-68-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59467-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,6 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59467-68:
(7*5)+(6*9)+(5*4)+(4*6)+(3*7)+(2*6)+(1*8)=174
174 % 10 = 4
So 59467-68-4 is a valid CAS Registry Number.

59467-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[7-chloro-5-(2-fluoro-phenyl)-2,3-dihydro-1H-benzo[e][1,4]diazepin-2-ylmethyl]-acetamide

1.2 Other means of identification

Product number -
Other names 2-acetaminomethyl-7-chloro-2,3-dihydro-5-(2-fluorophenyl)-1H-1,4-benzodiazepine

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:59467-68-4 SDS

59467-68-4Downstream Products

59467-68-4Relevant articles and documents

Convergent syntheses of carbon-13 labeled midazolam and 1′-hydroxymidazolam

Zhang, Yinsheng,Woo, Peter W.K.,Hartman, Jon,Colbry, Norman,Huang, Yun,Huang, Che C.

, p. 2087 - 2091 (2005)

For the purpose of drug interaction studies, the stable-isotope labeled [13C3]midazolam and its metabolite, 1′-hydroxy- [13C3]midazolam were synthesized in four and five steps in overall yields of 25.5% and 14.2%, from 7-chloro-5-(2-fluorophenyl)-2-(N- nitrosomethylamino)-3H-1,4-benzodiazepine, respectively, by a convergent synthesis, in which a key imidazoline ring formation was achieved by the facile reaction of [13C]2-aminomethyl-7-chloro-2,3-dihydro-5-(2- fluorophenyl)-1H-1,4-benzodiazepine with varying ethyl imidate hydrochlorides. The scrambling of C-3 and C-4 labeling in intermediate diamine, and consequently in the final products, as well as the formation of a Δ4,5 isomer of 1′-hydroxy-[13C3]midazolam was observed and explained.

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