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117120-88-4

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117120-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117120-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,2 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 117120-88:
(8*1)+(7*1)+(6*7)+(5*1)+(4*2)+(3*0)+(2*8)+(1*8)=94
94 % 10 = 4
So 117120-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N4O4S/c1-12-10(16)18-5-7-8(6-19-11(17)13-2)15(3)9(14-7)20-4/h5-6H2,1-4H3,(H,12,16)(H,13,17)

117120-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-methyl-5-(methylcarbamoyloxymethyl)-2-methylsulfanylimidazol-4-yl]methyl N-methylcarbamate

1.2 Other means of identification

Product number -
Other names -

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:117120-88-4 SDS

117120-88-4Upstream product

117120-88-4Downstream Products

117120-88-4Related news

Research papersStability of carmethizole (cas 117120-88-4) hydrochloride (NSC-602668), an experimental cytotoxic agent08/26/2019

The solution stability and degradation mechanism of Carmethizole HCl (1, NSC-602668), an experimental anti-cancer drug, were studied. An apparent pKa value of 4.2 at 25°C and ionic strength = 0.15 M (NaCl) was determined for 1 by potentiometric titration. The degradation 1 in aqueous solution p...detailed

A new synthesis of carmethizole (cas 117120-88-4) and related nitrogen analogues08/25/2019

A new efficient six-step synthesis of carmethizole, a novel bis-carbamate alkylating agent, and syntheses of related nitrogen analogues are described, using a key 4,5-disubstituted imidazole intermediate 8.detailed

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