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73882-21-0

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73882-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73882-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,8 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73882-21:
(7*7)+(6*3)+(5*8)+(4*8)+(3*2)+(2*2)+(1*1)=150
150 % 10 = 0
So 73882-21-0 is a valid CAS Registry Number.

73882-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-[3-(2,2-dimethylaziridin-1-yl)-1,4-dioxonaphthalen-2-yl]acetamide

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:73882-21-0 SDS

73882-21-0Downstream Products

73882-21-0Relevant articles and documents

Acid-catalysed, Nucleophile-catalysed and Thermal Decomposition of 2-Amino-3-(2',2'-dimethylaziridino)-1,4-naphthoquinone

Antonini, Ippolito,Claudi, Francesco,Cristalli, Gloria,Grifantini, Mario,Martelli, Sante

, p. 181 - 185 (2007/10/02)

The course of the thermal, acid-catalysed and iodide-catalysed decomposition of 2-amino-3-(2',2'-dimethylaziridino)-1,4-naphthoquinone (III) was investigated.Thermal and iodide-catalysed decompositions gave mainly 2,3-diamino-1,4-naphthoquinone (VI) and 2-amino-3-(2'-methylallylamino)-1,4-naphthoquinone (V) together with low amounts of 2,2-dimethyl-1,2,3,4,5,10-hexahydrobenzoquinoxaline (IV) and 2-isopropyl-1H-naphthoimidazole-4,9-dione (VII).The acid catalysed isomerization of the aziridinonaphthoquinone III with halohydric acids or with acetic acid readily gave the opening of the aziridine ring; the corresponding salts of 2-amino-3-(2'-haloisobutylamino)-1,4-naphthoquinones (VIIIa-c) and 2-amino-3-(2'-acetoxyisobutylamino)-1,4-naphthoquinone (X) were formed by cleavage of the carbon-nitrogen bond at the substituted carbon atom.Hypotheses on the mechanism of these reactions are given.

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