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941294-28-6

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941294-28-6 Usage

General Description

5-Bromo-4-cyclohexylpyrimidine is a chemical compound with the molecular formula C10H12BrN3. It is a pyrimidine derivative with a bromine atom substituted at the 5th position and a cyclohexyl group attached at the 4th position. 5-Bromo-4-cyclohexylpyrimidine is primarily used as a building block in the synthesis of pharmaceuticals and agrochemicals. It is known for its potential biological activities, including anticancer and antifungal properties. Additionally, it has been studied for its potential use as an inhibitor for certain enzymes and proteins. 5-Bromo-4-cyclohexylpyrimidine is a valuable compound in the field of medicinal and agricultural chemistry due to its versatile reactivity and biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 941294-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,1,2,9 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 941294-28:
(8*9)+(7*4)+(6*1)+(5*2)+(4*9)+(3*4)+(2*2)+(1*8)=176
176 % 10 = 6
So 941294-28-6 is a valid CAS Registry Number.

941294-28-6SDS

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 5-Bromo-4-cyclohexylpyrimidine

1.2 Other means of identification

Product number -
Other names 5-bromanyl-4-cyclohexyl-pyrimidine

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:941294-28-6 SDS

941294-28-6Downstream Products

941294-28-6Relevant articles and documents

Cross-dehydrogenative coupling of α-C(sp3)-H of ethers/alkanes with C(sp2)-H of heteroarenes under metal-free conditions

Ambala, Srinivas,Thatikonda, Thanusha,Sharma, Shweta,Munagala, Gurunadham,Yempalla, Kushalava Reddy,Vishwakarma, Ram A.,Singh, Parvinder Pal

, p. 11341 - 11350 (2015/11/27)

Here we have developed an effective metal-free dehydrogenative coupling method wherein α-oxyalkyl and alkyl radicals were generated from various ethers and alkanes to undergo coupling with a variety of electron-deficient heteroarenes such as un/substitute

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