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10132-28-2

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10132-28-2 Usage

General Description

2-(butylamino)pyrimidine is a chemical compound with the molecular formula C9H14N4. It is a pyrimidine derivative that contains a butylamino group attached to the second carbon atom of the pyrimidine ring. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 2-(butylamino)pyrimidine has the potential to act as a nucleoside analog, making it useful in the development of antiviral and anticancer drugs. Additionally, 2-(butylamino)pyrimidine has been studied for its potential biological activities, including its effects on cell growth and proliferation. Overall, this chemical compound has a range of potential applications in the field of pharmaceutical and agrochemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 10132-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,3 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10132-28:
(7*1)+(6*0)+(5*1)+(4*3)+(3*2)+(2*2)+(1*8)=42
42 % 10 = 2
So 10132-28-2 is a valid CAS Registry Number.

10132-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butylpyrimidin-2-amine

1.2 Other means of identification

Product number -
Other names butyl-pyrimidin-2-yl-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:10132-28-2 SDS

10132-28-2Upstream product

10132-28-2Relevant articles and documents

Ruthenium-Catalyzed Reductive Arylation of N-(2-Pyridinyl)amides with Isopropanol and Arylboronate Esters

Ronson, Thomas O.,Renders, Evelien,Van Steijvoort, Ben F.,Wang, Xubin,Wybon, Clarence C. D.,Prokopcová, Hana,Meerpoel, Lieven,Maes, Bert U. W.

supporting information, p. 482 - 487 (2019/01/04)

A new three-component reductive arylation of amides with stable reactants (iPrOH and arylboronate esters), making use of a 2-pyridinyl (Py) directing group, is described. The N-Py-amide substrates are readily prepared from carboxylic acids and PyNH2, and the resulting N-Py-1-arylalkanamine reaction products are easily transformed into the corresponding chlorides by substitution of the HN-Py group with HCl. The 1-aryl-1-chloroalkane products allow substitution and cross-coupling reactions. Therefore, a general protocol for the transformation of carboxylic acids into a variety of functionalities is obtained. The Py-NH2 by-product can be recycled.

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