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Benzenemethanol, 2-[[4-(trifluoromethyl)phenyl]methyl]-, also known as 2-[4-(trifluoromethyl)benzyl]benzenemethanol or 2-(4-trifluoromethylbenzyl)benzyl alcohol, is an organic compound with the molecular formula C15H13F3O. It is a colorless liquid at room temperature and is characterized by its distinct chemical structure, which includes a benzyl alcohol group attached to a benzene ring, with a trifluoromethyl group on the 4-position of the benzene ring. Benzenemethanol, 2-[[4-(trifluoromethyl)phenyl]methyl]- is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique properties and reactivity. It is also known for its potential applications in the development of new materials and as a building block in organic chemistry.

10324-25-1

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10324-25-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10324-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,2 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10324-25:
(7*1)+(6*0)+(5*3)+(4*2)+(3*4)+(2*2)+(1*5)=51
51 % 10 = 1
So 10324-25-1 is a valid CAS Registry Number.

10324-25-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(4-Trifluoromethyl-benzyl)-phenyl]-methanol

1.2 Other means of identification

Product number -
Other names -

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

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More Details:10324-25-1 SDS

10324-25-1Relevant academic research and scientific papers

Reductive ring opening of oxygen-containing benzo-fused heterocycles by an arene-catalysed lithiation

Yus, Miguel,Moreno, Benjamin,Foubelo, Francisco

, p. 1115 - 1118 (2007/10/03)

The reductive ring opening of phthalan and isochroman in a 8 mmol scale process, using a small excess of lithium (1.35 equiv) and a substoichiometric amount of DTBB (3 mol%), leads to functionalised organolithium compounds, which after reaction with (-)-m

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