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21017-20-9

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21017-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21017-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,1 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21017-20:
(7*2)+(6*1)+(5*0)+(4*1)+(3*7)+(2*2)+(1*0)=49
49 % 10 = 9
So 21017-20-9 is a valid CAS Registry Number.

21017-20-9SDS

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 ethyl 3-phenylsulfanylbut-2-enoate

1.2 Other means of identification

Product number -
Other names cis-3-Phenylthio-crotonsaeure-aethylester

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:21017-20-9 SDS

21017-20-9Relevant articles and documents

Three-component reactions of phosphorus ylides, thiophenols, and acetyl chloride for the synthesis of (β-thioacrylates)

Liu, Yunyun,Huang, Bin

, p. 926 - 929 (2016/07/06)

The facile synthesis of 2-thioacrylates has been realized via direct three-component reactions of thiophenols, Wittig reagents, and acetyl chloride. Under transition metal-free conditions, a class of 2-thioacrylates have been synthesized with fair to exce

Synthesis of deuterium-labeled derivatives of dimethylallyl diphosphate

Thulasiram, Hirekodathakallu V.,Phan, Richard M.,Rivera, Susan B.,Poulter, C. Dale

, p. 1739 - 1741 (2007/10/03)

Short practical syntheses for five deuterium-labeled derivatives of dimethylallyl diphosphate (DMAPP) useful for enzymological studies are reported. These include the preparation of the C1-labeled derivatives (R)-[1- 2H]3-methylbut-2-enyl diphosphate ((R)-[1-2H]1-OPP) and (S)-[1-2H]3-methylbut-2-enyl diphosphate ((S)-[1-2H]1-OPP) , the C2-labeled derivative [2-2H]3-methylbut-2-enyl diphosphate ([2-2H]1-OPP), and the methyl-labeled derivatives (E)-[4,4,4- 2H3]3-methylbut-2-enyl diphosphate ((E)-[4,4,4- 2H3]1-OPP) and (Z)-[4,4,4-2H 3]3-methyl-but-2-enyl diphosphate ((Z)-[4,4,4-2H 3]1-OPP).

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