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1,1,3,3-tetrafluoro-2-phenyl-propan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6302-09-6

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6302-09-6 Usage

Type of compound

Fluorinated alcohol

Stereochemistry

Chiral molecule with a non-superimposable mirror image

Applications

a. Synthesis of pharmaceuticals
b. Synthesis of agrochemicals
c. Synthesis of other fine chemicals

Unique properties

a. High selectivity and specificity in chemical reactions
b. Increased lipophilicity due to fluorinated structure
c. Enhanced stability due to fluorinated structure

Potential medical applications

a. Anti-inflammatory properties
b. Antioxidant properties

Check Digit Verification of cas no

The CAS Registry Mumber 6302-09-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6302-09:
(6*6)+(5*3)+(4*0)+(3*2)+(2*0)+(1*9)=66
66 % 10 = 6
So 6302-09-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H8F4O/c10-7(11)9(14,8(12)13)6-4-2-1-3-5-6/h1-5,7-8,14H

6302-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3,3-tetrafluoro-2-phenylpropan-2-ol

1.2 Other means of identification

Product number -
Other names 1,1,3,3-tetrafluoro-2-phenyl-propan-2-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:6302-09-6 SDS

6302-09-6Downstream Products

6302-09-6Relevant academic research and scientific papers

Difluoromethylation of carboxylic acids via the addition of difluorinated phosphorus ylide to acyl chlorides

Trifonov, Alexey L.,Levin, Vitalij V.,Struchkova, Marina I.,Dilman, Alexander D.

, p. 5304 - 5307 (2017)

A one-step protocol for the difluoromethylation of carboxylic acids is described. The reaction involves the interaction of intermediate acyl chlorides with in situ generated difluorinated phosphorus ylide Ph3P=CF2. Aromatic acids can be selectively transformed within one step either to bis-difluoromethylated alcohols or to difluorinated ketones depending on the particular reaction conditions. For bulky α-branched carboxylic acids, only ketones are produced.

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