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369638-71-1

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369638-71-1 Usage

Description

(5-Aminomethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester is a chemical compound that belongs to the class of carbamic acid esters. It is characterized by the presence of an aminomethyl group and a pyrazin-2-yl group, which contribute to its potential use in the modification and design of drug candidates. The tert-butyl ester group in the compound offers stability and protection during chemical reactions, making it a versatile and valuable component in the field of medicinal chemistry and drug discovery.

Uses

Used in Organic Synthesis:
(5-Aminomethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester is used as a building block for the synthesis of various biologically active compounds. Its unique functional groups facilitate the creation of a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (5-Aminomethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester is used as an intermediate in the development of new drugs. Its structural features make it a promising candidate for the design of novel therapeutic agents, particularly those targeting specific biological pathways or receptors.
Used in Medicinal Chemistry:
(5-Aminomethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester is employed as a versatile chemical in medicinal chemistry, where it can be utilized to modify and design potential drug candidates. Its aminomethyl and pyrazin-2-yl groups provide opportunities for further chemical modifications, enhancing the compound's potential for various therapeutic applications.
Overall, (5-Aminomethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester is a valuable compound with significant applications in organic synthesis, pharmaceutical research, and medicinal chemistry, making it an essential tool in the development of new and improved drugs for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 369638-71-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,9,6,3 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 369638-71:
(8*3)+(7*6)+(6*9)+(5*6)+(4*3)+(3*8)+(2*7)+(1*1)=201
201 % 10 = 1
So 369638-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N4O2/c1-10(2,3)16-9(15)14-8-6-12-7(4-11)5-13-8/h5-6H,4,11H2,1-3H3,(H,13,14,15)

369638-71-1SDS

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 tert-butyl N-[5-(aminomethyl)pyrazin-2-yl]carbamate

1.2 Other means of identification

Product number -
Other names (5-AMINOMETHYL-PYRAZIN-2-YL)-CARBAMIC ACID TERT-BUTYL ESTER

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:369638-71-1 SDS

369638-71-1Downstream Products

369638-71-1Relevant articles and documents

Non-covalent thrombin inhibitors featuring P3-heterocycles with P1-monocyclic arginine surrogates

Reiner, John E.,Siev, Daniel V.,Araldi, Gian-Luca,Cui, Jingrong Jean,Ho, Jonathan Z.,Reddy, Komandla Malla,Mamedova, Lala,Vu, Phong H.,Lee, Kuen-Shan S.,Minami, Nathaniel K.,Gibson, Tony S.,Anderson, Susanne M.,Bradbury, Annette E.,Nolan, Thomas G.,Semple, J. Edward

, p. 1203 - 1208 (2007/10/03)

Investigations on P2-P3-heterocyclic dipeptide surrogates directed towards identification of an orally bioavailable thrombin inhibitor led us to pursue novel classes of achiral, non-covalent P1-arginine derivatives. The design, synthesis, and biological activity of inhibitors NC1-NC30 that feature three classes of monocyclic P1-arginine surrogates will be disclosed: (1) (hetero)aromatic amidines, amines and hydroxyamidines, (2) 2-aminopyrazines, and (3) 2-aminopyrimidines and 2-aminotetrahydropyrimidines.

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