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3-(Chloromethyl)benzophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79128-88-4

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79128-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79128-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,2 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79128-88:
(7*7)+(6*9)+(5*1)+(4*2)+(3*8)+(2*8)+(1*8)=164
164 % 10 = 4
So 79128-88-4 is a valid CAS Registry Number.

79128-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(chloromethyl)phenyl]-phenylmethanone

1.2 Other means of identification

Product number -
Other names m-chloromethylbenzophenone

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:79128-88-4 SDS

79128-88-4Downstream Products

79128-88-4Relevant academic research and scientific papers

Photoinduced ω-bond dissociation of m-halomethylbenzophenones studied by laser photolysis techniques and DFT calculations. Substituted position effects

Yamaji, Minoru,Ogasawara, Michiyo,Kikuchi, Kazuhiro,Nakajima, Satoru,Tero-Kubota, Shozo,Marciniak, Bronislaw,Nozaki, Koichi

, p. 3268 - 3275 (2008/09/19)

Photochemical profiles of ω-cleavage of carbon-X (X = Br and Cl) bonds in m-bromo- and m-chloromethylbenzophenones (m-BMBP and m-CMBP) were investigated by laser photolysis techniques and DFT calculations. m-BMBP and m-CMBP were found to undergo ω-bond cleavage to yield the m-benzoylbenzyl radical (m-BBR) at 295 K, and the quantum yields were determined. No CIDEP signal was detected upon 308 nm laser photolysis of both the compounds. From these observations, it was inferred that the ω-bond of these m-halomethylbenzophenones (m-HMBP) cleaves in the lowest excited singlet state (S1(n,π*)) upon direct excitation. Upon triplet sensitization of acetone (Ac), the m-BBR formation was observed in transient absorption for an Ac-m-BMBP system, and an efficiency of the C-Br bond cleavage in the lowest triplet state (T1(n,π*)) of m-BMBP was determined. In contrast, formation of triplet m-CMBP was seen for an Ac-m-CMBP system. Absence of C-Cl bond cleavage in the triplet state of m-CMBP indicated the reactive state of m-CMBP for ω-cleavage is only the S 1(n,π*) state. Based on the efficiencies and DFT calculations for excited state energies, photoinduced ω-bond dissociation of m- and p-HMBPs was characterized. the Owner Societies.

Photoreactive benzoylphenylalanines and related peptides

-

, (2008/06/13)

Provided is a benzoylphenylalanine of the formula: STR1 wherein STR2 is in the m or p position; and Pr is a protecting group which is easily cleavable in the presence of a peptide bond by a mild acid or base. This benzoylphenylalanine group is incorporated into a peptide chain which can be attached to a solid substrate having a reactive hydrogen by exposure to low energy ultraviolet light.

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