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116137-73-6

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116137-73-6 Usage

General Description

2,4(1H,3H)-Pyrimidinedione, 6-butyl- is a chemical compound with the molecular formula C9H14N2O2. It is a derivative of pyrimidine and contains a butyl group attached to the sixth position of the pyrimidine ring. 2,4(1H,3H)-Pyrimidinedione, 6-butyl- has a variety of potential applications, including use as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It may also have biological activity and could be used as a building block in medicinal chemistry research. Additionally, 2,4(1H,3H)-Pyrimidinedione, 6-butyl- may have potential industrial uses and could be of interest to researchers in the fields of organic chemistry and chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 116137-73-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,3 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116137-73:
(8*1)+(7*1)+(6*6)+(5*1)+(4*3)+(3*7)+(2*7)+(1*3)=106
106 % 10 = 6
So 116137-73-6 is a valid CAS Registry Number.

116137-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dihydroxy-6-n-butylpyrimidine

1.2 Other means of identification

Product number -
Other names 6-butylpyrimidin-2,4-diol

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:116137-73-6 SDS

116137-73-6Relevant articles and documents

DIAMINOPYRIMIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF

-

, (2014/01/08)

The present invention provides a diaminopyrimidine derivative or its pharmaceutically acceptable salt, a process for the preparation thereof, a pharmaceutical composition comprising the same, and a use thereof. The diaminopyrimidine derivative or its pharmaceutically acceptable salt functions as a 5-HT4 receptor agonist, and therefore can be usefully applied for preventing or treating dysfunction in gastrointestinal motility, one of the gastrointestinal diseases, such as gastroesophageal reflux disease (GERD), constipation, irritable bowel syndrome (IBS), dyspepsia, post-operative ileus, delayed gastric emptying, gastroparesis, intestinal pseudo-obstruction, drug-induced delayed transit, or diabetic gastric atony.

DIAMINOPYRIMIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF

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Page/Page column 57, (2012/09/11)

The present invention provides a diaminopyrimidine derivative or its pharmaceutically acceptable salt, a process for the preparation thereof, a pharmaceutical composition comprising the same, and a use thereof. The diaminopyrimidine derivative or its pharmaceutically acceptable salt functions as a 5-HT4 receptor agonist, and therefore can be usefully applied for preventing or treating dysfunction in gastrointestinal motility, one of the gastrointestinal diseases, such as gastroesophageal reflux disease (GERD), constipation, irritable bowel syndrome (IBS), dyspepsia, post-operative ileus, delayed gastric emptying, gastroparesis, intestinal pseudo-obstruction, drug-induced delayed transit, or diabetic gastric atony.

Structure-Activity Relations. Part 12. Antibacterial Activity of a Series of 2,4-Diamino-6-substituted 5-(4-pyridylmethylamino)pyrimidines and 2,4-Diamino-5-(4-substituted benzylamino)pyrimidines.

Bowden, Keith,Bright, Andrew C.

, p. 514 - 539 (2007/10/02)

A series of 6-substituted 2,4-diamino-5-(4-pyridylamino)pyrimidines and of 2,4-diamino-5-(4-substituted benzylamino)pyrimidines has been prepared.Their antibacterial activity towards L. casei, S. aureus and E. coli has been investigated.These activities have been successfully correlated by Hansch-type relations.Dependence on both lipophilicity and electronic (polar) factors has been found.The results are related to the structure and interactions with the receptor.

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