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2227-70-5

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2227-70-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2227-70-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2227-70:
(6*2)+(5*2)+(4*2)+(3*7)+(2*7)+(1*0)=65
65 % 10 = 5
So 2227-70-5 is a valid CAS Registry Number.

2227-70-5 Well-known Company Product Price

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

  • (H51717)  2-(3-Methylphenyl)-4-phenylthiazole, 97%   

  • 2227-70-5

  • 1g

  • 774.0CNY

  • Detail
  • Alfa Aesar

  • (H51717)  2-(3-Methylphenyl)-4-phenylthiazole, 97%   

  • 2227-70-5

  • 5g

  • 2822.0CNY

  • Detail
  • Aldrich

  • (BOG00141)  4-Phenyl-2-(m-tolyl)thiazole  AldrichCPR

  • 2227-70-5

  • BOG00141-1G

  • 1,290.51CNY

  • Detail

2227-70-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-Methylphenyl)-4-phenyl-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 2-m-Methylphenyl-4-phenylthiazol

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:2227-70-5 SDS

2227-70-5Downstream Products

2227-70-5Relevant articles and documents

Br?nsted acid-promoted thiazole synthesis under metal-free conditions using sulfur powder as the sulfur source

Ni, Penghui,Tan, Jing,Li, Rong,Huang, Huawen,Zhang, Feng,Deng, Guo-Jun

, p. 3931 - 3935 (2020/02/04)

A Br?nsted acid-promoted sulfuration/annulation reaction for the one-pot synthesis of bis-substituted thiazoles from benzylamines, acetophenones, and sulfur powder has been developed. One C-N bond and multi C-S bonds were selectively formed in one pot. The choice of the Br?nsted acid was the key to the high efficiency of this transformation under metal-free conditions.

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