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4-Pyrimidinecarboxamide, 1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-, also known as Barbituric acid, is an organic compound with the chemical formula C6H8N2O3. It is a white crystalline solid that is derived from the parent compound pyrimidine. Barbituric acid is a key intermediate in the synthesis of barbiturates, a class of sedative and hypnotic drugs. It is formed by the condensation of urea with malonic acid, resulting in a molecule with two methyl groups at the 1 and 3 positions, and a carboxamide group at the 4 position. Barbituric acid is not itself psychoactive, but its derivatives, the barbiturates, have been widely used in medicine for their sedative, hypnotic, and anticonvulsant properties. However, due to their potential for abuse and dependence, the use of barbiturates has declined in favor of safer alternatives.

2019-20-7

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2019-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2019-20-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,1 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2019-20:
(6*2)+(5*0)+(4*1)+(3*9)+(2*2)+(1*0)=47
47 % 10 = 7
So 2019-20-7 is a valid CAS Registry Number.

2019-20-7SDS

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 1,3-dimethyluracil-6-carboxamide

1.2 Other means of identification

Product number -
Other names 1,3-Dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-carbonsaeure-amid

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:2019-20-7 SDS

2019-20-7Relevant academic research and scientific papers

Chemical models and their mechanistic implications for the transformation of 6-cyanouridine 5′-monophosphate catalyzed by orotidine 5′-monophosphate decarboxylase

Wu, Yuen-Jen,Liao, Chen-Chieh,Jen, Cheng-Hung,Shih, Yu-Chiao,Chien, Tun-Cheng

scheme or table, p. 4821 - 4823 (2010/08/22)

The reactions of 6-cyano-1,3-dimethyluracil have been studied as chemical models to illustrate the mechanism for the transformation of 6-cyanouridine 5′-monophosphate (6-CN-UMP) to barbiturate ribonucleoside 5′-monophosphate (BMP) catalyzed by orotidine 5′-monophosphate decarboxylase (ODCase). The results suggest that the Asp residue in the ODCase active site plays the role of a general base in the transformation.

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