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1H-Pyrrole-3-carboxamide, 4,5-dihydro-4,5-dioxo-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116046-46-9

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116046-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116046-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,4 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 116046-46:
(8*1)+(7*1)+(6*6)+(5*0)+(4*4)+(3*6)+(2*4)+(1*6)=99
99 % 10 = 9
So 116046-46-9 is a valid CAS Registry Number.

116046-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dioxo-2-phenyl-1H-pyrrole-3-carboxamide

1.2 Other means of identification

Product number -
Other names 1H-Pyrrole-3-carboxamide,4,5-dihydro-4,5-dioxo-2-phenyl

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:116046-46-9 SDS

116046-46-9Downstream Products

116046-46-9Relevant academic research and scientific papers

ACYLATION OF Α-SCF3 SUBSTITUTED Β-CARBONYL ACETIC ACID AND THIACETIC ACID DERIVATIVES WITH OXALYL CHLORIDE

Zankowska-Jasinska, W.

, p. 85 - 94 (2007/10/02)

α-CF3S-substituted β-ketoacidamides, nitriles, thioamides and their Schiff bases are synthesised and their reactions with oxalyl chloride are investigated.As a new phenomenon the elimination of the CF3S group during cyclisation to substituted 2,3,5-trioxo-1,4-oxazepine (7), 4-pyrroline-2,3-dione (9) and oxalyl (10) is observed.Factors influencing this course of the reaction and mechanism of product formation are discussed.

OXALYL CHLORIDE IN FURAN- AND 1H-PYRROLE-2,3-DIONE SYNTHESES

Zankowska-Jasinska, Wanda,Golus, Janusz,Kamela, Zofia,Kolasa, Anna

, p. 141 - 148 (2007/10/02)

Condensation of benzoylacetic acid amide and its imino derivative with oxalyl chloride yielded furan-2,3-dione 1 and 1H-pyrrole-2,3-dione 2 derivatives, respectively.The structure of the latter was proved by an analogous condensation of β-aminocinnamic ni

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