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300394-89-2

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300394-89-2 Usage

Description

5-Bromo-N-isobutylpyridin-2-amine, with the molecular formula C11H16BrN2, is a brominated derivative of N-isobutylpyridin-2-amine. It is an organic compound classified under anilines and substituted anilines. 5-broMo-N-isobutylpyridin-2-aMine is known for its versatile chemical properties, making it a valuable component in the synthesis of various products.

Uses

Used in Pharmaceutical Industry:
5-Bromo-N-isobutylpyridin-2-amine is used as an intermediate in the synthesis of medicinal drugs. Its unique structure allows it to be a key component in the development of new pharmaceuticals, contributing to the advancement of medical treatments.
Used in Agrochemical Development:
In the agrochemical industry, 5-Bromo-N-isobutylpyridin-2-amine serves as a building block for the creation of various agrochemicals. Its incorporation into these products can enhance their effectiveness in agricultural applications, such as pest control and crop protection.
Used in Fine Chemicals Production:
5-Bromo-N-isobutylpyridin-2-amine is also utilized in the production of fine chemicals. Its presence in these specialty chemicals can improve their performance and quality, catering to specific industrial needs.
Used in Research Applications:
Due to its distinctive chemical properties, 5-Bromo-N-isobutylpyridin-2-amine is employed in various research applications. It aids scientists in studying chemical reactions and exploring new avenues in chemical synthesis and compound development.
Precaution:
Given its potential health and environmental hazards, 5-Bromo-N-isobutylpyridin-2-amine should be handled with care. Proper safety measures and disposal methods must be adhered to, ensuring the well-being of individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 300394-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,0,3,9 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 300394-89:
(8*3)+(7*0)+(6*0)+(5*3)+(4*9)+(3*4)+(2*8)+(1*9)=112
112 % 10 = 2
So 300394-89-2 is a valid CAS Registry Number.

300394-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-N-(2-methylpropyl)pyridin-2-amine

1.2 Other means of identification

Product number -
Other names 5-bromo-N-isobutylpyridin-2-amine

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:300394-89-2 SDS

300394-89-2Downstream Products

300394-89-2Relevant articles and documents

Inverting Conventional Chemoselectivity in Pd-Catalyzed Amine Arylations with Multiply Halogenated Pyridines

Keylor, Mitchell H.,Niemeyer, Zachary L.,Sigman, Matthew S.,Tan, Kian L.

supporting information, p. 10613 - 10616 (2017/08/15)

A new catalyst system capable of selective chloride functionalization in the Pd-catalyzed amination of 3,2- and 5,2- Br/Cl-pyridines is reported. A reaction optimization strategy employing ligand parametrization led to the identification of 1,1′-bis[bis(dimethylamino)phosphino]ferrocene "DMAPF", a readily available yet previously unutilized diphosphine, as a uniquely effective ligand for this transformation.

The Chemistry of N-Substituted Benzotriazoles. Part 4. A Novel and Versatile Method for the Mono-N-alkylation of Aromatic and Heteroaromatic Amines

Katritzky, Alan R.,Rachwal, Stanislaw,Rachwal, Bogumila

, p. 805 - 810 (2007/10/02)

Mono-N-alkylation of aromatic and heteroaromatic amines is achieved in high yield by NaBH4 reduction of the adducts formed from benzotriazole, aliphatic aldehydes and the amines.Reaction of the same adducts with Grignard reagents gives N-(secondary alkyl)arylamines.Carboxy groups need no protection and nitro groups are unaffected.Adenine is mono-N-alkylated in high yield.

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