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1,3-di(phenyl-d5)-2-propan-d4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84752-07-8

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84752-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84752-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,5 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84752-07:
(7*8)+(6*4)+(5*7)+(4*5)+(3*2)+(2*0)+(1*7)=148
148 % 10 = 8
So 84752-07-8 is a valid CAS Registry Number.

84752-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-di(phenyl-d5)-2-propan-d4-one

1.2 Other means of identification

Product number -
Other names Dibenzylketon-d14

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:84752-07-8 SDS

84752-07-8Upstream product

84752-07-8Relevant academic research and scientific papers

Micellar Systems as ''Supercages'' for Reactions of Geminate Radical Pairs. Magnetic Effects

Turro, Nicholas J.,Weed, Gregory C.

, p. 1861 - 1868 (1983)

The photochemistry of dibenzyl ketone (DBK) and other molecules capable of producing benzyl radicals and substituted benzyl radicals has been investigated in micellar systems.The cage effect (percent of unscavengeable radical pairs produced by photolysis) was measured under a variety of conditions, and the results are compared with those obtained in homogeneous organic solvents.For example, parameters such as mean occupancy of ketone, detergent type and concentration, O2 concentration, additives, temperature, applied magnetic field, and pressure have been varied and investigated as to their influence on the magnitude of cage effect.In addition to modifying its environment, structural modification of the DBK by incorporation of 2H and 13C isotopes, hydrophobic groups, and heavy atoms was performed to investigate the impact of these variations on the cage effect in micellar systems.Isotopic substitution of 2H or 13C leads to results on both the quantum yields for reactions and on the percent cage that were consistent with expectations of magnetic isotope effects.Hydrophobic groups substituted in the 4-position of DBK were found to cause a substantial increase in the cage effect and yet retain the magnetic-field-dependent character found in the parent DBK.Incorporation of Br in the 4-position of DBK was found to enhance the cage effect but at the same time cause the cage effect to become magnetic field independent.Substitution of α-naphthyl for phenyl in DBK also produced magnetic-field-independent behavior, in addition to a dramatic decrease in the efficiency of photolysis.

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