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

16513-76-1

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16513-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16513-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,1 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16513-76:
(7*1)+(6*6)+(5*5)+(4*1)+(3*3)+(2*7)+(1*6)=101
101 % 10 = 1
So 16513-76-1 is a valid CAS Registry Number.

16513-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-cyanophenyl) benzoate

1.2 Other means of identification

Product number -
Other names 3-cyanophenyl benzoate

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:16513-76-1 SDS

16513-76-1Downstream Products

16513-76-1Relevant academic research and scientific papers

Energy-Transfer-Mediated Photocatalysis by a Bioinspired Organic Perylenephotosensitizer HiBRCP

Zhang, Yan,Xia, Mingze,Li, Min,Ping, Qian,Yuan, Zhenbo,Liu, Xuanzhong,Yin, Huimin,Huang, Shuping,Rao, Yijian

, p. 15284 - 15297 (2021/11/01)

Energy transfer plays a special role in photocatalysis by utilizing the potential energy of the excited state through indirect excitation, in which a photosensitizer determines the thermodynamic feasibility of the reaction. Bioinspired by the energy-transfer ability of natural product cercosporin, here we developed a green and highly efficient organic photosensitizer HiBRCP (hexaisobutyryl reduced cercosporin) through structural modification of cercosporin. After structural manipulation, its triplet energy was greatly improved, and then, it could markedly promote the efficient geometrical isomerization of alkenes from the E-isomer to the Z-isomer. Moreover, it was also effective for energy-transfer-mediated organometallic catalysis, which allowed realization of the cross-coupling of aryl bromides and carboxylic acids through efficient energy transfer from HiBRCP to nickel complexes. Thus, the study on the relationship between structural manipulation and their photophysical properties provided guidance for further modification of cercosporin, which could be applied to more meaningful and challenging energy-transfer reactions.

Influence of substituents on the infrared stretching frequencies of carbonyl group in esters of benzoic acid

Nummert, Vilve,Travnikova, Oksana,Vahur, Signe,Leito, Ivo,Piirsalu, Mare,Maeemets, Vahur,Koppel, Ivar,Koppel, Ilmar A.

, p. 654 - 663 (2008/02/08)

Infrared spectra of 25 substituted phenyl esters of benzoic acid C 6H5CO2C6H4-X (X=H, 3-Cl, 3-F, 3-CN, 3-NO2, 3-CH3, 3-OH, 3-NH2, 4-Cl, 4-F, 4-NO2, 4-CN, 4-

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