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143230-69-7

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  • 4,5-Oxazoledione, 2-phenyl-, 4-[[4-chloro-3-[(2,2,3,3,3-pentafluoropropoxy)methyl]phenyl]hydrazone]

    Cas No: 143230-69-7

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143230-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143230-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,3 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 143230-69:
(8*1)+(7*4)+(6*3)+(5*2)+(4*3)+(3*0)+(2*6)+(1*9)=97
97 % 10 = 7
So 143230-69-7 is a valid CAS Registry Number.

143230-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-4,5-oxazoledione 4-[4-chloro-3-(2,2,3,3,3,-pentafluoropropoxymethyl)-phenylhydrazone]

1.2 Other means of identification

Product number -
Other names 2-phenyl-4,5-oxazoledione 4-[4-chloro-3-(2,2,3,3,3-pentafluoropropoxy)methylphenyl]hydrazone

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:143230-69-7 SDS

143230-69-7Relevant articles and documents

Process for the manufacture of 2-phenyl-4,5-oxazoledione 4-phenylhydrazone derivatives

-

, (2008/06/13)

A process for manufacturing derivatives of 2-phenyl-4,5-oxazoledione 4-phenylhyrazone is disclosed. The process comprises reacting a derivative of a benezenediazonium salt, a hippuric acid derivative, and acetic anhydride in the presence of a neutralizing agent to effect the cyclization reaction for the formation of the oxazolone ring and the succeeding diazo-coupling reaction. The process does not require the conventional separate, independent step for the preparation of a solution of a hippuric acid derivative and acetic anhydride, thus eliminating the quick heating and quenching procedures and further avoiding the loss of the hippuric acid derivative due to decomposition of the oxazolone derivative. There is thus obtained a high yield of the desired product in a short period of time.

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