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Benzene, 1,1'-(1-fluoroethylidene)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74185-82-3

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74185-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74185-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,8 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74185-82:
(7*7)+(6*4)+(5*1)+(4*8)+(3*5)+(2*8)+(1*2)=143
143 % 10 = 3
So 74185-82-3 is a valid CAS Registry Number.

74185-82-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-fluoro-1-phenylethyl)benzene

1.2 Other means of identification

Product number -
Other names -

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:74185-82-3 SDS

74185-82-3Upstream product

74185-82-3Downstream Products

74185-82-3Relevant academic research and scientific papers

Evidence for Carbocation Intermediates in the TiO2-Catalyzed Photochemical Fluorination of Carboxylic Acids

Lai, Cuiwei,Kim, Yeong Il,Wang, Chong Mou,Mallouk, Thomas E.

, p. 1393 - 1399 (2007/10/02)

Laser flash photolysis/transient absorbance spectroscopy was used to determine the mechanism of photo-Kolbe fluorination of carboxylic acids, RCOOH --> RF, at colloidal TiO2 suspensions in acetonitrile.Transient absorption spectra of Ph3C(+), Ph3C(*), Ph2CH(*) and Ph2CH(+) were observed from the photooxidation of Ph3CCOOH and Ph2CHCOOH at TiO2 using 355-nm excitation.Transient decays, monitored in the presence and absence of fluoride ions, showed that the carbocations reacted rapidly with fluoride, but the neutral radicals did not.By varying the laser intensity, it wa s found that the photooxidation of Ph3CCOOH to Ph3C(*) at TiO2 occured via a single-photon process, while the formation of of Ph3C(+) required two photons.This finding is in agreement with the parabolic light intensity dependence of initial reaction rates in bulk photolysis experiments.Although fluoride is strongly adsorbed on the TiO2 surface in acetonitrile solution, the oxidizing power of photogenerated holes could be increased by coordinating HF to F(-), and therefore the threshold for oxidative photochemical fluorination was extented to more positive potentials.In this way less easily oxidized carboxylic acids RCOOH could be converted to RF.

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