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93787-99-6

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93787-99-6 Usage

General Description

6-ethoxy-1,3-dimethyl-pyrimidine-2,4-dione is a chemical compound with the molecular formula C7H10N2O3. It is a pyrimidine derivative and belongs to the class of organic compounds known as pyrimidinediones. 6-ethoxy-1,3-dimethyl-pyrimidine-2,4-dione has a molecular weight of 166.17 g/mol and a melting point of 109-110°C. It is typically used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, it has been studied for its potential anticonvulsant and antihypertensive properties. However, it also carries potential health hazards and should be handled and used with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 93787-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,8 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93787-99:
(7*9)+(6*3)+(5*7)+(4*8)+(3*7)+(2*9)+(1*9)=196
196 % 10 = 6
So 93787-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2O3/c1-4-13-7-5-6(11)9(2)8(12)10(7)3/h5H,4H2,1-3H3

93787-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-ethoxy-1,3-dimethylpyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 6-ethoxy-1,3-dimethyl-1H-pyrimidine-2,4-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:93787-99-6 SDS

93787-99-6Downstream Products

93787-99-6Relevant articles and documents

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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