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16513-72-7

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16513-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16513-72-7 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 16513-72:
(7*1)+(6*6)+(5*5)+(4*1)+(3*3)+(2*7)+(1*2)=97
97 % 10 = 7
So 16513-72-7 is a valid CAS Registry Number.

16513-72-7SDS

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 (4-cyanophenyl) benzoate

1.2 Other means of identification

Product number -
Other names benzoic acid p-cyanophenyl 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:16513-72-7 SDS

16513-72-7Relevant articles and documents

Discovery and characterization of a novel perylenephotoreductant for the activation of aryl halides

Guo, Baodang,Huang, Shuping,Li, Jia,Li, Min,Liu, Xuanzhong,Rao, Yijian,Wu, Yawen,Yin, Huimin,Yuan, Zhenbo,Zhang, Yan

, p. 111 - 120 (2021/06/16)

To develop a photocatalyst with catalytical activity for substrates with low reactivities is always highly desired. Herein, based on the principle of structure–property relationships, we rationally designed the natural product cercosporin, the naturally occurring perylenequinonoid pigment, to develop a novel organic perylenephotoreductant, hexacetyl reduced cercosporin (HARCP), through structural manipulation. Compared with cercosporin, HARCP shows prominent electrochemical and photophysical characteristics with greatly improved photoreductive activity, fluorescence lifetime and fluorescence quantum yield. These properties allowed HARCP as a powerful photoreductant to efficiently realize a series of benchmark reactions, including photoreduction, alkoxylation and hydroxylation to construct C–H and C–O bonds using aryl halides as substrates under mild conditions, all of which have never been achieved by the same photocatalyst. Thus, this study well supports the notion that the principle between structural manipulation and photocatalytic activity is of great significance to design customized photocatalysts for photoredox chemistry.

Visible light-mediated transition metal-free esterification of amides with boronic acids

Ding, Hao,Qi, Wan-Ying,Zhen, Jing-Song,Ding, Qiuping,Luo, Yong

supporting information, (2020/10/02)

A novel strategy for visible light-mediated esterification of amides with boronic acids in air has been described. This method is characterized by mild reaction conditions and low cost owing to no need of any catalyst, which implies high potential utility in late-stage functionalization of amide drugs and materials.

Hexaacyl reductive cercosporin photocatalyst, and preparation method and application thereof

-

Paragraph 0085-0087, (2020/11/12)

The invention discloses a hexacyloyl reductive cercosporin photocatalyst and preparation and application thereof, belonging to the technical field of preparation methods and organic synthesis of catalysts. The preparation method comprises the following steps: adding anhydride into a mixture of cercosporin, a reducing agent and alkali, carrying out stirring at room temperature for 1-3 hours, addinganhydride, continuing reacting for 1-3 hours, and carrying out suction filtration, extraction, concentration and column chromatography purification to obtain the catalyst. The catalyst provided by the invention can catalyze reduction, coupling and other photochemical reactions of halogenated hydrocarbons, and has strong reaction activity and industrialization prospects.

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