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4-ethyl-1,2,4-triazine-3,5(2H,4H)-dione is an organic compound with the chemical formula C5H7N3O2. It is a derivative of the triazine family, characterized by a six-membered heterocyclic ring containing three nitrogen atoms. This specific compound features an ethyl group attached to the 4-position of the triazine ring and two carbonyl groups at the 3 and 5 positions. It is a white crystalline solid and is used as an intermediate in the synthesis of various chemical products, including herbicides and pharmaceuticals. Due to its reactivity and potential applications, it is important to handle 4-ethyl-1,2,4-triazine-3,5(2H,4H)-dione with care, following proper safety protocols.

1627-31-2

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1627-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1627-31-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1627-31:
(6*1)+(5*6)+(4*2)+(3*7)+(2*3)+(1*1)=72
72 % 10 = 2
So 1627-31-2 is a valid CAS Registry Number.

1627-31-2SDS

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 4-ethyl-2H-1,2,4-triazine-3,5-dione

1.2 Other means of identification

Product number -
Other names 3-Ethyl-6-aza-uracil

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:1627-31-2 SDS

1627-31-2Upstream product

1627-31-2Downstream Products

1627-31-2Relevant academic research and scientific papers

Anticoccidial derivatives of 6 azauracil. I. Enhancement of activity by benzylation of nitrogen 1. Observations on the design of nucleotide analogues in chemotherapy

Mylari,Miller,Howes Jr.,Figdor,Lynch,Koch

, p. 475 - 483 (2007/10/09)

Benzylation of 6-azauracil at N-1 (which corresponds to the point of attachment of the ribose phosphate unit in pyrimidine nucleotides) has been found to augment its anticoccidial activity fourfold. The high potency of 1-benzyl-6-azauracil is ascribed to a combination of intrinsic activity, efficient oral absorption, and a moderate rate of excretion. Metabolism experiments using 1-benzyl-6-azauracil labeled with 14C in the heterocycle and (separately) in the side chain showed that, in the drug accounted for, no cleavage had occurred. Additional activity increases were achieved by introducing small, electron-withdrawing substituents in the meta and/or para position(s) of the benzyl group. One of the most active derivatives, 1-(3-cyanobenzyl)-6-azauracil, is about 16 times as potent as 6-azauracil.

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