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4-AMINOMETHYL-PYRIDIN-3-YLAMINE, with the molecular formula C7H10N2, is an organic compound that falls under the category of amines. It is a versatile building block in the synthesis of various products, including pharmaceuticals, agrochemicals, and other organic compounds. Its utility extends to research and development for the creation of new drugs and materials, making it a valuable component across the chemical, pharmaceutical, and agricultural industries.

144288-49-3

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144288-49-3 Usage

Uses

Used in Pharmaceutical Industry:
4-AMINOMETHYL-PYRIDIN-3-YLAMINE is used as a chemical intermediate for the synthesis of various pharmaceuticals. It plays a crucial role in the development of new drugs due to its ability to form a wide range of chemical structures, contributing to the discovery of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 4-AMINOMETHYL-PYRIDIN-3-YLAMINE is utilized as a precursor in the production of various agrochemicals. Its involvement in the synthesis of these compounds aids in the development of effective solutions for pest control and crop protection.
Used in Research and Development:
4-AMINOMETHYL-PYRIDIN-3-YLAMINE is used as a research compound for the exploration of new materials and drug candidates. Its presence in the lab setting is instrumental in advancing scientific knowledge and facilitating the innovation of new chemical entities with potential applications in medicine and other fields.
Used in Chemical Industry:
Within the chemical industry, 4-AMINOMETHYL-PYRIDIN-3-YLAMINE serves as a versatile building block for the synthesis of a variety of organic compounds. Its adaptability in chemical reactions makes it a valuable asset in the creation of new chemical products and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 144288-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,8 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144288-49:
(8*1)+(7*4)+(6*4)+(5*2)+(4*8)+(3*8)+(2*4)+(1*9)=143
143 % 10 = 3
So 144288-49-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H9N3/c7-3-5-1-2-9-4-6(5)8/h1-2,4H,3,7-8H2

144288-49-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(aminomethyl)pyridin-3-amine

1.2 Other means of identification

Product number -
Other names 3-Amino-4-pyridinemethanamine

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:144288-49-3 SDS

144288-49-3Relevant academic research and scientific papers

2-Aminomethylphenylamine as a novel scaffold for factor Xa inhibitor

Mochizuki, Akiyoshi,Nagata, Tsutomu,Kanno, Hideyuki,Suzuki, Makoto,Ohta, Toshiharu

, p. 1623 - 1642 (2011/04/21)

We have been researching orally active factor Xa inhibitor for a long time. We explored the new diamine linker using effective ligands to obtain a new attractive original scaffold 2-aminomethylphenylamine derivative. Compound 1D showed very strong in vitro and in vivo factor Xa inhibitory activity, as well as favorable PK profiles in po administration to monkeys.

Alkylamino derivatives of 4-aminomethylpyridine as inhibitors of copper-containing amine oxidases

Bertini, Vincenzo,Buffoni, Franca,Ignesti, Giovanni,Picci, Nevio,Trombino, Sonia,Iemma, Francesca,Alfei, Silvana,Pocci, Marco,Lucchesini, Francesco,De Munno, Angela

, p. 664 - 670 (2007/10/03)

The first substratelike, reversible inhibitors of different copper amine oxidases (CAOs) with IC50 (M) as low as 2.0 × 10-8 corresponding to derivatives of 4-aminomethylpyridine with alkoxy (1a-d), alkylthio (2a,b), and alkylamino (3

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