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4H-Pyrrolo[2,3-d]-1,2,3-thiadiazole-4-carboxylic acid, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

500136-13-0

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500136-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 500136-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,1,3 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 500136-13:
(8*5)+(7*0)+(6*0)+(5*1)+(4*3)+(3*6)+(2*1)+(1*3)=80
80 % 10 = 0
So 500136-13-0 is a valid CAS Registry Number.

500136-13-0SDS

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 methyl pyrrolo[2,3-d]thiadiazole-4-carboxylate

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:500136-13-0 SDS

500136-13-0Relevant academic research and scientific papers

Investigation of the regioselectivity of the Hurde-Mori reaction for the formation of bicyclic1,2,3-thiadiazoles

Turner, Martin,Linder, Thomas,Schnürch, Michael,Mihovilovic, Marko D.,Stanetty, Peter

experimental part, p. 5472 - 5478 (2010/08/13)

A series of new pyrrolo[d][1,2,3]thiadiazole carboxylates and 5,6-dihydro-4H-cyclopenta[d][1,2,3]thia-diazoles has been synthesized via the HurdeMori reaction.The regioselectivity of the cyclization has been studied and trends were established to predict the cyclization direction to afford bicyclic 1,2,3-thiadiazoles.Effects promoting and disfavoring the reaction have also been investigated to guide the synthesis of scaffolds of this type.

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