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2267-65-4

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2267-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2267-65-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,6 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2267-65:
(6*2)+(5*2)+(4*6)+(3*7)+(2*6)+(1*5)=84
84 % 10 = 4
So 2267-65-4 is a valid CAS Registry Number.

2267-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names phenyl 1,2,2,2,-tetrafluoroethyl ketone

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:2267-65-4 SDS

2267-65-4Relevant articles and documents

NUCLEOPHILIC REACTIONS OF FLUOROOLEFINS. II. REGIOSELECTIVITY AND ELIMINATION-ADDITION COMPETITION IN THE REACTION OF 1-PHENYLPENTAFLUOROPROPENES WITH SODIUM ETHOXIDE

Dmowski, Wojciech

, p. 201 - 220 (1982)

1-Phenylpentafluoropropene and its para-substituted analogs 1 are susceptible to nucleophilic attack at both vinylic carbon atoms C-1 and C-2.They react with ethanolic sodium ethoxide to give predominantly substitution products, 1-ethoxy-1-phenyltetrafluo

Dephosphorylation of 1-Substituted F-1-Alkenyl Phosphates with Diisobutylaluminium Hydride. A New Highly Efficient Method for Generating F-Alkyl Ketone Aluminium(III) Enolates

Ishihara, Takashi,Yamaguchi, Koichi,Kuroboshi, Manabu

, p. 1191 - 1194 (2007/10/02)

1-Substituted F-1-alkenyl phosphates, prepared easily from F-alkyl ketones, were treated with diisobutylaluminium hydride in tetrahydrofuran at 0 deg C for 5 min or at room temperature for 30 min to generate quantitetively the corresponding ketone alumini

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