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158715-14-1

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158715-14-1 Usage

General Description

2-phenyl-6-trifluoromethyl-pyrimidin-4-ol is a chemical compound with a molecular formula C12H7F3N2O. It is a pyrimidine derivative with a phenyl and a trifluoromethyl group attached to the 2 and 6 positions, respectively. The compound has a hydroxyl group at the 4 position of the pyrimidine ring. It is a potentially useful molecule in medicinal chemistry, as pyrimidine derivatives have been shown to exhibit various pharmacological activities, including antiviral, antibacterial, and antitumor properties. The trifluoromethyl group also contributes to the compound's lipophilicity and stability, making it a valuable building block for drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 158715-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,7,1 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 158715-14:
(8*1)+(7*5)+(6*8)+(5*7)+(4*1)+(3*5)+(2*1)+(1*4)=151
151 % 10 = 1
So 158715-14-1 is a valid CAS Registry Number.

158715-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-6-(trifluoromethyl)-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 2-Phenyl-6-trifluoromethyl-pyrimidin-4-ol

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:158715-14-1 SDS

158715-14-1Downstream Products

158715-14-1Relevant articles and documents

Synthesis 2-substituted 6-fluoroalkylpyrimidin-4(3H)-ones and -pyrimidines

Guan, Hui-Ping,Hu, Qiao-Sheng,Hu, Chang-Ming

, p. 997 - 1001 (1996)

Treatment of ethyl α-fluoroalkylacetates 1 or ethyl 3-fluoroalkyl-2-iodoacrylates 2 under mild conditions with amidine affords 2-substituted 6-fluoroalkylpyrimidin-4(3H)-ones 4, 5, 6, 7 in excellent yields, while α-fluoroalkyl alkyl ketones or α-fluoroalk

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