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Benzenemethanol, 4-chloro-a-phenyl-a-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1996-66-3

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1996-66-3 Usage

Chemical Class

Benzyl alcohols

Physical Appearance

White to off-white solid

Solubility

Insoluble in water, soluble in organic solvents

Primary Use

Key intermediate for synthesis of other organic compounds

Applications

Pharmaceuticals
Agrochemicals
Academic research chemicals

Potential

Building block for new materials and substances

Value

Widely used in organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 1996-66-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1996-66:
(6*1)+(5*9)+(4*9)+(3*6)+(2*6)+(1*6)=123
123 % 10 = 3
So 1996-66-3 is a valid CAS Registry Number.

1996-66-3Downstream Products

1996-66-3Relevant academic research and scientific papers

Gas/Liquid-Phase Micro-Flow Trifluoromethylation using Fluoroform: Trifluoromethylation of Aldehydes, Ketones, Chalcones, and N-Sulfinylimines

Hirano, Kazuki,Gondo, Satoshi,Punna, Nagender,Tokunaga, Etsuko,Shibata, Norio

, p. 406 - 410 (2019/02/13)

A micro-flow nucleophilic trifluoromethylation of carbonyl compounds using gaseous fluoroform was developed. This method also allows the first micro-flow transformation of N-sulfinylimines into trifluoromethyl amines with excellent diastereoselectivity. To demonstrate the synthetic utility of this micro-flow synthesis, the formal micro-flow synthesis of Efavirenz is described.

METHOD FOR PRODUCING TRIFLUOROMETHYL GROUP-CONTAINING ALCOHOLS

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Paragraph 0060; 0063; 0064, (2018/04/10)

PROBLEM TO BE SOLVED: To provide a method for producing trifluoromethyl group-containing alcohols useful as synthetic intermediates for medicines and agrochemicals. SOLUTION: This invention relates to a method for producing trifluoromethyl group-containing alcohols expressed by a formula (2), comprising: making carbonyl compounds expressed by a formula (1) react with trifluoromethane in an organic solvent in the presence of polyvalent ethers and potassium tert-butoxide, or kalium hexamethyldisilazide. (R1 and R2 are each independently a phenyl group etc.; R2 may combine with R1, to form a ring, and both R1 and R2 are not hydrogen atoms). SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

METHOD FOR PRODUCING TRIFLUOROMETHYL GROUP-CONTAINING ALCOHOLS

-

Paragraph 0029-0031; 0033-0035, (2017/02/02)

PROBLEM TO BE SOLVED: To provide a method for producing CF3 group-containing alcohols useful as production intermediates for medicines and agrochemicals. SOLUTION: The method for producing CF3 group-containing alcohols represented by formula (2) comprises

Organocatalyzed Trifluoromethylation of Ketones and Sulfonyl Fluorides by Fluoroform under a Superbase System

Okusu, Satoshi,Hirano, Kazuki,Tokunaga, Etsuko,Shibata, Norio

, p. 581 - 585 (2015/10/20)

Fluoroform (HCF3, HFC-23) is a side product in the manufacture of polytetrafluoroethylene (Teflon). Despite its attractive properties, taming HCF3 for trifluoromethylation is quite problematic owing to its low acidity and the labilit

The rhodium-catalysed 1,2-addition of arylboronic acids to aldehydes and ketones with sulfonated S-Phos

White, James R.,Price, Gareth J.,Plucinski, Pawel K.,Frost, Christopher G.

supporting information; experimental part, p. 7365 - 7368 (2010/03/03)

The rhodium-catalysed 1,2-addition of arylboronic acids to aryl aldehydes has been accomplished in high yield using sulfonated S-Phos, a water-soluble biaryl phosphine ligand which allows for catalyst recycling. The catalytic protocol has also been successful in the challenging arylation of ketones.

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