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5-bromo-3-methylpyrimidine-2,4(1H,3H)-dione is a heterocyclic organic compound characterized by a pyrimidine ring structure, which is a six-membered aromatic ring containing four carbon atoms and two nitrogen atoms. This specific compound features a bromine atom at the 5th position, a methyl group at the 3rd position, and two carbonyl groups (C=O) at the 2nd and 4th positions. The compound is a dione, indicating the presence of two carbonyl groups, which contribute to its reactivity and potential applications in various chemical reactions. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

6832-03-7

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6832-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6832-03-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6832-03:
(6*6)+(5*8)+(4*3)+(3*2)+(2*0)+(1*3)=97
97 % 10 = 7
So 6832-03-7 is a valid CAS Registry Number.

6832-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-3-methyl-1H-pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-bromo-3-methyl-2,4(1H,3H)pyrimidinedione

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:6832-03-7 SDS

6832-03-7Upstream product

6832-03-7Relevant academic research and scientific papers

NOVEL HETEROCYCLIC COMPOUNDS AND USE THEREOF IN MEDICINE AND IN COSMETICS

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Paragraph 0412, (2018/03/25)

The invention relates to novel heterocyclic compounds of general formula (I), as well as their pharmaceutically acceptable salts, and their enantiomers. The invention also relates to the use thereof as a medicinal product, preferably in the prevention and/or treatment of inflammatory diseases with a neurogenic component or use thereof as a cosmetic. The compounds of the present invention act as antagonists of the CGRP-R receptor.

Mechanisms of Bromination of Uracil Derivatives. 5. Reaction of Uracil and 5-Bromouracil via Their Anions in Weakly Acidic Aqueous Solution

Tee, Oswald S.,Berks, Charles G.

, p. 830 - 835 (2007/10/02)

The rates of reaction of bromine with uracil, 1-methyluracil, 3-methyluracil, 1,3-dimethyluracil, 5-bromouracil, and 5-bromo-1,3-dimethyluracil have been measured in acidic, aqueous solutions (pH 0-5).For those derivatives having a methyl group at N1 the observed second-order rate constants are invariant with acidity, whereas for those derivatives having hydrogen at N1 they increase with decreasing acidity.These results suggest that reaction upon the anions of uracil, 3-methyluracil, and 5-bromouracil predominates at higher pH.The mechanistic implications of these findings are discussed.

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