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3,4-Pyridinediamine,N3-(phenylmethyl)-, also known as N-(phenylmethyl)pyridine-3,4-diamine, is a chemical compound with the molecular formula C12H12N4. It is a derivative of pyridine, characterized by the presence of two amine groups and a phenylmethyl group attached to the pyridine ring. 3,4-Pyridinediamine,N3-(phenylmethyl)is utilized in the synthesis of various pharmaceuticals and organic compounds, making it a significant entity in the realm of organic chemistry and pharmaceutical research.

75115-28-5

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75115-28-5 Usage

Uses

Used in Pharmaceutical Industry:
3,4-Pyridinediamine,N3-(phenylmethyl)is used as an intermediate in the synthesis of pharmaceuticals for the treatment of various diseases, including cancer. Its unique structure allows for the development of drugs that can target specific biological pathways, offering potential therapeutic benefits.
Used in Dye and Pigment Production:
3,4-Pyridinediamine,N3-(phenylmethyl)is also utilized in the production of dyes and pigments due to its chemical properties that contribute to coloration. Its application in this industry aids in the creation of a wide range of colorants for various uses, including textiles, plastics, and printing inks.
Used in Chemical Research and Development:
3,4-Pyridinediamine,N3-(phenylmethyl)plays a crucial role in the research and development of new chemical processes and materials. Its versatility in chemical reactions and potential to form new compounds makes it an important tool for scientists and researchers working on innovative projects in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 75115-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,1 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75115-28:
(7*7)+(6*5)+(5*1)+(4*1)+(3*5)+(2*2)+(1*8)=115
115 % 10 = 5
So 75115-28-5 is a valid CAS Registry Number.

75115-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N3-Benzylpyridine-3,4-diamine

1.2 Other means of identification

Product number -
Other names 3-N-benzylpyridine-3,4-diamine

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:75115-28-5 SDS

75115-28-5Relevant academic research and scientific papers

Rapid construction of imidazopyridines from ortho-haloaminopyridines

Li, Chaomin,Chen, Lily,Steinhuebel, Dietrich,Goodman, Andrew

supporting information, p. 2708 - 2712 (2016/06/09)

A practical strategy for the preparation of imidazopyridine derivatives from ortho-haloaminopyridines utilizing a two-step C-N coupling/cyclization reaction sequence has been developed. This procedure provides rapid and efficient access to many medicinally interesting imidazopyridine compounds and related imidazopyrazine/purine heterocycles.

Na2S2O4: A versatile reagent for the one-pot synthesis of 2-aryl-1h-imidazo[4,5-c]pyridines from 4-amino-3- nitropyridine and aldehydes via reductive cyclization

Dubey,Chowdary,Ramesh,Reddy, P. V. V. Prasada

, p. 697 - 708 (2011/03/19)

A highly efficient and versatile method for the synthesis of 2-aryl-1H-imidazo[4,5-c]pyridines 3 was achieved in one step via reductive cyclization of 4-amino-3-nitro-pyridines 4 with aromatic aldehydes in the presence of Na2S2O

PREPARATION OF 2-ARYL-SUBSTITUTED IMIDAZOPYRIDINES AND IMIDAZOPYRIDINES

Yutilov, Yu. M.,Shcherbina, L. I.

, p. 529 - 535 (2007/10/02)

It is proposed that sulfur be used as the oxidizing agent in the synthesis of 2-arylimidazopyridines from o-diaminopyridines and aromatic (heteroaromatic) aldehydes.Benzyl alcohols and benzylpyridinium salts can be used in place of aldehydes. 2-Phenylimid

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