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6645-65-4

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6645-65-4 Usage

Physical state

White solid

Usage

Intermediate for the synthesis of various organic compounds

Applications

Production of dyes, pharmaceuticals, and polymers

Role

Reactive agent in the formation of complex organic molecules

Potential use

Anti-cancer drugs and other medicinal applications

Field of relevance

Organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 6645-65-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,4 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6645-65:
(6*6)+(5*6)+(4*4)+(3*5)+(2*6)+(1*5)=114
114 % 10 = 4
So 6645-65-4 is a valid CAS Registry Number.

6645-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Terephthalsaeure-bis-phenylhydrazid

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:6645-65-4 SDS

6645-65-4Downstream Products

6645-65-4Relevant articles and documents

Use of acylhydrazine- and acylhydrazone-type ligands to promote CuI-catalyzed C-N cross-coupling reactions of aryl bromides with N-heterocycles

Li, Liuyi,Zhu, Lei,Chen, Dagui,Hu, Xuelei,Wang, Ruihu

, p. 2692 - 2696 (2011)

A series of ten acylhydrazine- and acylhydrazone-type ligands were designed and synthesized. Their electronic and steric properties were easily modified and tuned by varying the substituents in the vicinity of the acylhydrazine and acylhydrazone units. The effect of ligands on the catalytic activity of Ullmann reactions was assessed by using a combination of these ligands with CuI. The catalytic system is very efficient for the C-N coupling reaction of azoles with aryl and heteroaryl bromides. A simple and efficient procedure for copper-catalyzed C-N cross-coupling reactions between aryl bromides and NH-containingheterocycles is illustrated. Readily available acylhydrazine- and acylhydrazone-typeligands promote the reaction.

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