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4-(1,2,3-THIADIAZOL-4-YL)PYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102253-71-4

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102253-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102253-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,5 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102253-71:
(8*1)+(7*0)+(6*2)+(5*2)+(4*5)+(3*3)+(2*7)+(1*1)=74
74 % 10 = 4
So 102253-71-4 is a valid CAS Registry Number.

102253-71-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H51821)  4-(4-Pyridyl)-1,2,3-thiadiazole, 96%   

  • 102253-71-4

  • 250mg

  • 568.0CNY

  • Detail
  • Alfa Aesar

  • (H51821)  4-(4-Pyridyl)-1,2,3-thiadiazole, 96%   

  • 102253-71-4

  • 1g

  • 1705.0CNY

  • Detail

102253-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-pyridin-4-ylthiadiazole

1.2 Other means of identification

Product number -
Other names Pyridine,4-(1,2,3-thiadiazol-4-yl)

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:102253-71-4 SDS

102253-71-4Relevant academic research and scientific papers

TBAI-Catalyzed Reaction between N-Tosylhydrazones and Sulfur: A Procedure toward 1,2,3-Thiadiazole

Chen, Jiangfei,Jiang, Yan,Yu, Jin-Tao,Cheng, Jiang

, p. 271 - 275 (2016)

A TBAI-catalyzed reaction between N-tosyl hydrazone and sulfur was developed, leading to 1,2,3-thiadiazoles in moderate to good yields. It represents a facile and practical procedure to access thiadiazole under metal-free conditions. This procedure serves

Determination of the transglycosidation activity of NAD+ glycohydrolases with 4-(2′-alkyl-sulfanyl-vinyl)-pyridine derivatives generating chromophoric NAD+ analogs

Pacaud, Karine,Tritsch, Denis,Burger, Alain,Biellmann, Jean-Francois

, p. 288 - 305 (2007/10/03)

The base exchange of nicotinamide with pyridine derivatives 1a-5a, catalyzed by pig brain NAD+ glycohydrolase and ADP-ribosyl cyclase from Aplysia californica, generated the corresponding NAD+ analogs 1b-5b. These analogs exhibited a high absorbance band in the visible region. The transglycosidation rate was determined by monitoring the absorbance increase. Among the tested derivatives, (E)-4-[2-(methylsulfanyl)-vinyl]-pyridine 1a was the most suitable substrate for pig brain NAD+ glycohydrolase while 4-[1,3]-dithiolan-2-ylidenemethyl-pyridine 3a was the most efficient for ADP-ribosyl cyclase from A. californica.

Cephalosporin derivatives and salts thereof

-

, (2008/06/13)

Novel cephalosporin derivatives and salts thereof are disclosed. These compounds exhibit excellent antimicrobial activity against a wide variety of Gram-negative and Gram-positive bacteria and also have other excellent characteristics as a medicine such as stability and low toxicity. These compounds can be administered in a form of subcutaneous, intravenous or intramuscular injections.

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