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5456-76-8

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5456-76-8 Usage

Chemical class

Nitrofuran compound

Physical state

Yellow solid

Potential applications

Pharmaceutical and agricultural industries

Known properties

Antimicrobial and antiparasitic

Biological activities

May have similar biological activities to other nitrofuran compounds

Concerns

Potential toxicity and carcinogenicity

Use restrictions

Restricted in food production in many countries

Further research

Needed to fully understand potential uses and risks

Check Digit Verification of cas no

The CAS Registry Mumber 5456-76-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5456-76:
(6*5)+(5*4)+(4*5)+(3*6)+(2*7)+(1*6)=108
108 % 10 = 8
So 5456-76-8 is a valid CAS Registry Number.

5456-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-nitrofuran-2-yl)propan-1-one

1.2 Other means of identification

Product number -
Other names Ethyl-2-(5-nitrofuryl)-keton

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:5456-76-8 SDS

5456-76-8Downstream Products

5456-76-8Relevant articles and documents

Vicarious nucleophilic substitution of hydrogen in nitroderivatives of five-membered heteroaromatic compounds

Makosza, Mieczyslaw,Kwast, Ewa

, p. 8339 - 8354 (2007/10/02)

Nitro derivatives of thiophene, furan and pyrrole react with carbanions containing leaving groups giving products of replacement of hydrogen with functionalized alkyl substituents. Many specific features of this reaction are discussed.

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