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4-Fluorobenzoic acid phenacyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55153-22-5

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55153-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55153-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55153-22:
(7*5)+(6*5)+(5*1)+(4*5)+(3*3)+(2*2)+(1*2)=105
105 % 10 = 5
So 55153-22-5 is a valid CAS Registry Number.

55153-22-5SDS

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 Phenacyl-p-fluorbenzoat

1.2 Other means of identification

Product number -
Other names 4-FLUOROBENZOIC ACID PHENACYL ESTER

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:55153-22-5 SDS

55153-22-5Downstream Products

55153-22-5Relevant academic research and scientific papers

I2/TBHP-mediated oxidative coupling of ketones and toluene derivatives: a facile method for the preparation of α-benzoyloxy ketones

Chen, Cui,Liu, Weibing,Zhou, Peng,Liu, Hailing

, p. 20394 - 20397 (2017/04/19)

An efficient oxidative approach was developed for the α-benzoyloxylation of ketones using tert-butyl hydroperoxide (TBHP). This process provided facile access to a wide range of α-benzoyloxy ketones in good to excellent yields via the direct oxidative α-benzoyloxylation of a structurally diverse series of ketones using simple arylmethane compounds.

KINETICS OF REACTION OF TRIETHYLAMMONIUM CARBOXYLATES WITH α-HALOGENOCARBONYL COMPOUNDS IN ORGANIC SOLVENTS. REACTION OF BENZOATES AND PHENOXYACETATES WITH PHENACYL BROMIDE IN ACETONE

Pillay, M. Krishna,Kannan, K.,Ramasubramanian, P.

, p. 3899 - 3908 (2007/10/02)

The kinetics of the reaction of phenacyl bromide with triethylammonium p-substituted benzoates and phenoxyacetates at 25 deg C, 30 deg C and 35 deg C in acetone suggest a rigid cyclic transition state involving a hydrogen bonded ion-pair as the active nuc

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