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Ethyl 4-aminopyrimidine-5-carboxylate is a substituted pyrimidine derivative that serves as an essential intermediate in the synthesis of various compounds, including Thiamine (T344185) analogues. It is characterized by its unique chemical structure, which contributes to its role in the formation of complex molecules.
[Data of usage]:
Used in Pharmaceutical Industry:
Ethyl 4-aminopyrimidine-5-carboxylate is used as a synthetic intermediate for the production of Thiamine (T344185) analogues, which are essential for various biological processes and have potential therapeutic applications.
Used in Chemical Synthesis:
Ethyl 4-aminopyrimidine-5-carboxylate is used as a key building block in the synthesis of a wide range of chemical compounds, particularly those with potential applications in the pharmaceutical, agrochemical, and material science industries. Its unique structure allows for further functionalization and modification to create novel molecules with specific properties and functions.
Used in Research and Development:
As a substituted pyrimidine, ethyl 4-aminopyrimidine-5-carboxylate is utilized in research and development for the exploration of new chemical reactions, the design of novel molecules, and the investigation of their biological activities. Its versatility as a synthetic intermediate makes it a valuable tool in the advancement of scientific knowledge and the development of new technologies.

65195-35-9

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65195-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65195-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,9 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65195-35:
(7*6)+(6*5)+(5*1)+(4*9)+(3*5)+(2*3)+(1*5)=139
139 % 10 = 9
So 65195-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H9N3O2/c1-2-12-7(11)5-3-9-4-10-6(5)8/h3-4H,2H2,1H3,(H2,8,9,10)

65195-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-Aminopyrimidine-5-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl4-Aminopyrimidine-5-carboxylate

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:65195-35-9 SDS

65195-35-9Relevant academic research and scientific papers

Compounds for modulating TRPV3 function

-

Page/Page column `46, (2016/11/24)

The present application relates to compounds and methods for treating pain and other conditions related to TRPV3.

A method for the reductive scission of heterocyclic thioethers

Graham, Thomas H.,Liu, Wensheng,Shen, Dong-Ming

supporting information; experimental part, p. 6232 - 6235 (2012/01/03)

A mild, chemoselective, and generally high-yielding method for the reductive scission of heterocyclic thioethers is described. Suitable heterocycles have a thioether substituent at the 2-position relative to a ring heteroatom. The convenient and straightforward method is demonstrated with reactants which are not compatible with the standard Raney nickel conditions such as sulfides, sulfones, and thiophenes. In addition, benzyl esters, benzyl amides, and benzyl carbamates are tolerated by the reductive reaction conditions.

Compounds for modulating TRPV3 function

-

Page/Page column 46, (2010/11/28)

The present application relates to compounds and methods for treating pain and other conditions related to TRPV3.

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