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27472-40-8

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27472-40-8 Usage

Structure

A 1,2-propanedione molecule with a 1H-pyrrol-2-yl group attached

Appearance

Unknown, but likely a solid or liquid depending on the conditions

Odor

Sweet, caramel-like

Uses

a. Flavoring agent in the food industry
b. Fragrance in perfumes and personal care products
c. Intermediate in the synthesis of pharmaceutical drugs

Safety

Can be hazardous if not properly handled; should be used in accordance with safety guidelines

Regulatory Information

Unknown, but likely subject to various regulations depending on its use and location

Environmental Impact

Unknown, but like all chemicals, should be disposed of properly to minimize environmental harm.

Check Digit Verification of cas no

The CAS Registry Mumber 27472-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,4,7 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27472-40:
(7*2)+(6*7)+(5*4)+(4*7)+(3*2)+(2*4)+(1*0)=118
118 % 10 = 8
So 27472-40-8 is a valid CAS Registry Number.

27472-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1H-pyrrol-2-yl)-1,2-propanedione

1.2 Other means of identification

Product number -
Other names 1-(1H-Pyrrol-2-yl)-propane-1,2-dione

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:27472-40-8 SDS

27472-40-8Downstream Products

27472-40-8Relevant articles and documents

Copper-catalyzed TEMPO oxidative cleavage of 1,3-diketones and β-keto esters for the synthesis of 1,2-diketones and α-keto esters

Zhou, Peng-Jun,Li, Cheng-Kun,Zhou, Shao-Fang,Shoberu, Adedamola,Zou, Jian-Ping

, p. 2629 - 2637 (2017/04/03)

A copper-catalyzed efficient and practical method has been developed for the synthesis of 1,2-diketones and α-keto esters. TEMPO was used as a radical initiator and scavenger, oxidizing the cleavage of α-methylene of 1,3-diketones and β-keto esters to form 1,2-diketones and α-keto esters. This method provided a general way for the formation of 1,2-dicarbonyl compounds.

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