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2-(2H-tetrazol-5-yl)-4H-chromen-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33543-91-8

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33543-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33543-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,4 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33543-91:
(7*3)+(6*3)+(5*5)+(4*4)+(3*3)+(2*9)+(1*1)=108
108 % 10 = 8
So 33543-91-8 is a valid CAS Registry Number.

33543-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2H-tetrazol-5-yl)chromen-4-one

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:33543-91-8 SDS

33543-91-8Downstream Products

33543-91-8Relevant academic research and scientific papers

Production process of 2-(tetrazol-5-yl)-4-oxo-4H-benzopyran

-

, (2008/06/13)

There is disclosed a process for producing a 2-(tetrazol-5-yl)-4-oxo-4H-benzopyran of general formula (1): STR1 which comprises reacting a hydroxyacetophenone of general formula (2): STR2 with a tetrazole compound of general formula (3): STR3 in the presence of a base in a solvent composed mainly of at least one selected from hydrocarbons, halogenated hydrocarbons and alcohols, and then treating the reaction mixture under acidic conditions.

A direct and high yielding route to 2-(5-tetrazolyl) substituted benzopyran-4-ones: Synthesis of pranlukast

Geen, Graham R.,Giles, Robert G.,Grinter, Trevor J.,Hayler, John D.,Howie, Simon L. B.,Johnson, Graham,Mann, Inderjit S.,Novack, Vance J.,Oxley, Paul W.,Quick, John K.,Smith, Neil

, p. 1065 - 1073 (2007/10/03)

A direct and high yielding route to 2-(5-tetrazolyl)benzopyran-4-ones 1, including pranlukast 1a is described. This involves the Claisen condensation reaction between the relevant hydroxyacetophenone 2 and the ethyl ester of tetrazole-2-carboxylic acid 5 to give the 1,3-diketone 6, which is then cyclised to give the desired benzopyran-4-ones 1.

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