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Thiazole, 5-methyl-2-(2-propenyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154776-22-4

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154776-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154776-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,7,7 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 154776-22:
(8*1)+(7*5)+(6*4)+(5*7)+(4*7)+(3*6)+(2*2)+(1*2)=154
154 % 10 = 4
So 154776-22-4 is a valid CAS Registry Number.

154776-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Allyl-5-methyl-1,3-thiazole

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:154776-22-4 SDS

154776-22-4Upstream product

154776-22-4Downstream Products

154776-22-4Relevant academic research and scientific papers

Allylation of Azoles with Allyltributyltin via Unstable N-(Alkoxycarbonyl)azolium Salts

Itoh, Takashi,Hasegawa, Hiroshi,Nagata, Kazuhiro,Ohsawa, Akio

, p. 1319 - 1325 (1994)

The one-pot reactions of imidazoles with allyltributyltin in the presence of alkyl chloroformates gave 2-allyl-1,3-bis(alkoxycarbonyl)-4-imidazolines in good yields.The reactions of thiazoles and oxazoles also proceeded in a similar manner.The instability of the intermediary quaternary salts required the nucleophiles to be added simultaneously with the chloroformate.Therefore, the reaction was specific for allyltributyltin, since it doesn't react with the carbonyl group of chloroformates.The dihydro allyl adducts thus obtained were aromatized with potassium ferricyanide under basic conditions to afford the corresponding 2-allylazoles.

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