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21842-28-4

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21842-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21842-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,4 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21842-28:
(7*2)+(6*1)+(5*8)+(4*4)+(3*2)+(2*2)+(1*8)=94
94 % 10 = 4
So 21842-28-4 is a valid CAS Registry Number.

21842-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 14,15-dioxa-7-aza-dispiro[5.1.5.2]pentadecane

1.2 Other means of identification

Product number -
Other names 1,1'-peroxy-dicyclohexyl amine

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:21842-28-4 SDS

21842-28-4Upstream product

21842-28-4Relevant articles and documents

Preparation method of 11-cyanoundecanoic acid

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Paragraph 0030; 0031; 0033; 0034; 0036; 0037; 0039; 0040, (2019/05/08)

The invention relates to a preparation method of 11-cyanoundecanoic acid. 1,1'-peroxidation dicyclohexylamine (PXA) is subjected to a self-decomposition reaction under the effect of a rare earth metalcompound and a free radical initiator, thus the 11-cyanoundecanoic acid is obtained in a high-selectivity mode, and the PXA is generated by cyclohexanone through oxyamination. According to the process line, raw materials are simple and easy to obtain, the disadvantages that an existing process is difficult to control under the high-temperature condition and low in reaction selectivity, and products are difficult to separate are avoided, and the simple and convenient method is provided for preparation of the 11-cyanoundecanoic acid.

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