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21562-06-1

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21562-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21562-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,6 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21562-06:
(7*2)+(6*1)+(5*5)+(4*6)+(3*2)+(2*0)+(1*6)=81
81 % 10 = 1
So 21562-06-1 is a valid CAS Registry Number.

21562-06-1SDS

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 3-(3-methoxyphenyl)-1-methyl-1-nitrosourea

1.2 Other means of identification

Product number -
Other names 3-(m-Methoxyphenyl)-1-methyl-1-nitrosourea

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:21562-06-1 SDS

21562-06-1Downstream Products

21562-06-1Relevant articles and documents

Kinetics and Mechanism of Decomposition of N-Methyl-N'-aryl-N-nitrosoureas and Related Compounds in Aqueous Buffer Solution

Yoshida, Kitaro,Yano, Kazuyuki

, p. 2200 - 2203 (2007/10/02)

The decomposition reactions of N-methyl-N'-aryl-N-nitrosoureas (1) and of N,N'-dimethyl-N'-aryl-N-nitrosoureas (2) were studied kinetically in phosphate buffer solution.All nitrosoureas 1 were easily hydrolyzed even under conditions and the rates of hydrolysis were found to be proportional to the hydroxide ion concentration over pH range 5.4-7.6.General base catalysis by buffer components was negligible. The reaction was subjected to the elimination mechanism in which an abstraction of the urcido proton was involved as an initial step.On the other hand, nitrosoureas 2 had no significant reactivity under the same conditions.

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