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83329-71-9

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83329-71-9 Usage

Structure

Linear structure with two imidazole rings attached to a butanedione backbone

Derivative

Imidazole, a five-membered heterocyclic ring compound containing nitrogen

Applications

Building block for synthesizing various biologically active compounds and pharmaceuticals

Field of use

Medicinal chemistry, drug development targeting specific biological pathways

Additional uses

Research and development in biochemistry and molecular biology

Check Digit Verification of cas no

The CAS Registry Mumber 83329-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,2 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83329-71:
(7*8)+(6*3)+(5*3)+(4*2)+(3*9)+(2*7)+(1*1)=139
139 % 10 = 9
So 83329-71-9 is a valid CAS Registry Number.

83329-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-di(imidazol-1-yl)butane-1,4-dione

1.2 Other means of identification

Product number -
Other names 1H,1'H-1,1'-succinyl-bis-imidazole

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:83329-71-9 SDS

83329-71-9Downstream Products

83329-71-9Relevant articles and documents

Effect of sodium naphthalenide, a key SET reagent, on trifluoroacetyl derivatives

Banerji, Avijit,Bandyopadhyay, Debasish,Basak, Bidyut,Sur, Kumar R.,Paul, Jyoti N.,Banerji, Julie,Chatterjee, Asima

, p. 7033 - 7035 (2007/10/03)

Aromatic trifluoroacetyl derivatives on treatment with single electron transfer (SET) reagent, sodium naphthalenide, yield symmetrical defluorinated dimers, whereas for aliphatic trifluoroacetyl compounds the reaction usually fails. Investigations have been made for different substituents as well as for similar types of chloro and bromo compounds to establish the scope of the reaction.

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