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5-Pyrimidinemethanol, 4-amino-2-ethyl-, also known as 4-amino-2-ethyl-5-pyrimidinemethanol, is an organic compound with the chemical formula C7H11N3O. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring with four carbon atoms and two nitrogen atoms. The molecule features an amino group (-NH2) at the 4-position, an ethyl group (-CH2CH3) at the 2-position, and a hydroxymethyl group (-CH2OH) at the 5-position. 5-Pyrimidinemethanol, 4-amino-2-ethyl- is of interest in the field of organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and functional groups.

876-21-1

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876-21-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876-21-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 876-21:
(5*8)+(4*7)+(3*6)+(2*2)+(1*1)=91
91 % 10 = 1
So 876-21-1 is a valid CAS Registry Number.

876-21-1SDS

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-amino-2-ethylpyrimidin-5-yl)methanol

1.2 Other means of identification

Product number -
Other names 5-pyrimidinemethanol,4-amino-2-ethyl

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:876-21-1 SDS

876-21-1Upstream product

876-21-1Downstream Products

876-21-1Relevant academic research and scientific papers

Synthetic method for 2-ethyl-4-amino-5-hydroxymethyl pyrimidine

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Paragraph 0025; 0026; 0027; 0028; 0029, (2016/12/01)

The invention provides a synthetic method for 2-ethyl-4-amino-5-hydroxymethyl pyrimidine. The synthetic method comprises the following steps: dissolving a 2-ethyl-4-amino-pyrimidine ethyl formate solution in a reaction solvent, adding Lewis acid as a catalyst, adding a boron reagent as a reducing agent, and reacting to reduce 2-ethyl-4-amino-pyrimidine ethyl formate into the 2-ethyl-4-amino-5-hydroxymethyl pyrimidine. The method provided by the invention is low in cost, simple in reaction condition, simple and convenient in operation process, and is suitable to apply to large-scale industrial production.

FLUOROETHYL THIAMINE OR SALTS THEREOF AND APPLICATION THEREOF IN PREPARATION OF ANTICOCCIDIAL DRUGS

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Paragraph 0020; 0021; 0022, (2015/05/26)

The present invention discloses a fluoroethyl thiamine or salts thereof and application thereof in preparation of anticoccidial drugs. The structural formula of the fluoroethyl thiamine or salts thereof is shown as Formula (I). The fluoroethyl thiamine or

Fluoroethyl thiamine or salts thereof and application thereof in preparation of anticoccidial drugs

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Page/Page column 3-4, (2015/09/22)

The present invention discloses a fluoroethyl thiamine or salts thereof and application thereof in preparation of anticoccidial drugs. The structural formula of the fluoroethyl thiamine or salts thereof is shown as Formula (I). The fluoroethyl thiamine or

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