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17626-75-4

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17626-75-4 Usage

Chemical Properties

clear colorless to yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 17626-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,2 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17626-75:
(7*1)+(6*7)+(5*6)+(4*2)+(3*6)+(2*7)+(1*5)=124
124 % 10 = 4
So 17626-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NS/c1-2-3-6-7-4-5-8-6/h4-5H,2-3H2,1H3

17626-75-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (A11574)  2-n-Propylthiazole, 99%   

  • 17626-75-4

  • 5g

  • 571.0CNY

  • Detail
  • Alfa Aesar

  • (A11574)  2-n-Propylthiazole, 99%   

  • 17626-75-4

  • 25g

  • 2399.0CNY

  • Detail

17626-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Propylthiazole

1.2 Other means of identification

Product number -
Other names 2-propyl-1,3-thiazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:17626-75-4 SDS

17626-75-4Relevant articles and documents

Preparation method of 2-alkyl substituted thiazole compound

-

Paragraph 0055-0058, (2021/06/06)

The invention discloses a preparation method of a 2-alkyl substituted thiazole compound, which comprises the following steps: oxidizing 2-alkyl thiothiazole into 2-alkyl sulfonyl thiazole, mixing the 2-alkyl sulfonyl thiazole with a Grignard reagent, reacting the mixture at 0-5 DEG C, heating the mixture to room temperature to continue the reaction; then adding an acid solution and continuously reacting the components at room temperature to obtain a 2-alkyl substituted thiazole compound, wherein the structural formula of the 2-alkyl thiothiazole is that a Grignard reagent of the 2-alkyl sulfonyl thiazole is RCH2MgX, R1 is selected from C1-C4 alkyl groups, R is selected from H and C1-C4 alkyl groups, and X is halogen. According to the present invention, the use of the expensive palladium catalyst and the ligand is avoided, the use of the poor safety butyl lithium reagent is avoided, the ultra-low temperature of-78 DEG C is not required, the cheap and easily available 2-alkylthiothiazole is adopted as the starting material, the 2-alkyl substituted thiazole compound can be prepared under the milder condition, and the method is suitable for the industrial production.

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