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21367-02-2

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21367-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21367-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,6 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21367-02:
(7*2)+(6*1)+(5*3)+(4*6)+(3*7)+(2*0)+(1*2)=82
82 % 10 = 2
So 21367-02-2 is a valid CAS Registry Number.

21367-02-2SDS

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 1-acryloyloxymethyl-3-cyclohexene

1.2 Other means of identification

Product number -
Other names Acrylsaeure-cyclohex-3-enylmethylester

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:21367-02-2 SDS

21367-02-2Relevant articles and documents

Method for preparing (methyl)acrylic acid-3,4-epoxycyclohexyl methyl ester by microchannel reactor

-

Paragraph 0051; 0052, (2019/04/27)

The invention discloses a method for preparing (methyl) acrylic acid-3,4-epoxycyclohexyl methyl ester by a microchannel reactor. The method is characterized in that firstly, 3-cyclohexene-1-methanol and (methyl)acryloyl chloride are used as raw materials; esterification reaction is performed in the microchannel reactor to prepare an intermediate of (methyl)acrylic acid-3-cyclohexenyl methyl ester;then, peroxyacetic acid is used as an oxidizing agent; chlorohydrocarbon is used as a reaction medium; selective epoxidation reaction is performed in the microchannel reactor to prepare a target product. The esterification reaction temperature is low; the side reactions are few; the efficiency is high; the aftertreatment is simple; an in-situ method is used; peroxyacetic acid is prepared; meanwhile, olefin epoxidation reaction is performed; the technological process is easy to operate; the reaction yield is high; the product purity is high; the operation of the product separation process is simple; the method is suitable for continuous production; when a curing resin composition prepared by the product is used, a good cured matter with high sealing performance and chemical resistant performance on a base material can be obtained, and can be suitable for being used in the field of electronic materials.

SYNTHESIS AND STRUCTURE OF ACRYLOYLOXYMETHYL- AND 1-ACETOXYMETHYL-3,4-EPOXYCYCLOHEXANES

Batog, A. E.,Zaitsev, S. Yu.,Kiryushina, N. P.,Zaitseva, V. V.

, p. 76 - 79 (2007/10/02)

1-Acryloyloxymethyl- and 1-acetoxymethyl-3,4-epoxycyclohexanes were synthesized, and their structures were studied.It was shown that these compounds are cis- and trans-epoxy conformers and can take part in complex formation with acrylonitrile and with certain polar solvents.

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