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15814-25-2

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15814-25-2 Usage

Chemical class

Alcohols

Pharmaceutical industry use

Drug intermediate or active pharmaceutical ingredient

Studied properties

Anti-inflammatory and analgesic

Potential treatment

Various diseases

Application

Building block in organic synthesis for production of other pharmaceuticals and fine chemicals

Importance

Significant compound in pharmaceutical and chemical industries

Check Digit Verification of cas no

The CAS Registry Mumber 15814-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,1 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15814-25:
(7*1)+(6*5)+(5*8)+(4*1)+(3*4)+(2*2)+(1*5)=102
102 % 10 = 2
So 15814-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H11F3O2/c1-6(14)9(15)7-3-2-4-8(5-7)10(11,12)13/h2-6,9,14-15H,1H3

15814-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(trifluoromethyl)phenyl]propane-1,2-diol

1.2 Other means of identification

Product number -
Other names 1-(meta-trifluoromethylphenyl)-1,2-propanediol

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:15814-25-2 SDS

15814-25-2Relevant articles and documents

Asymmetric syntheses of (S)-Fenfluramine using Sharpless Epoxidation Methods

Goument, Bertrand,Duhamel, Lucette,Mauge, Robert

, p. 171 - 188 (2007/10/02)

We describe one synthesis of (S)-fenfluramine and several syntheses of its precursors (R)- and (S)-1-(meta-trifluoromethylphenyl)propan-2-ols.They were obtained from the asymmetric epoxidation of the primary allylic alcohol 5 and from the kinetic resolution with asymmetric epoxidation of teh secondary allylic alcohol 6.

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