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58753-28-9

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58753-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58753-28-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,5 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58753-28:
(7*5)+(6*8)+(5*7)+(4*5)+(3*3)+(2*2)+(1*8)=159
159 % 10 = 9
So 58753-28-9 is a valid CAS Registry Number.

58753-28-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzoylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names benzoyl-3 cyclohexanone

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:58753-28-9 SDS

58753-28-9Downstream Products

58753-28-9Relevant articles and documents

Synthesis of 3-benzoylcyclohexanone, a key intermediate for the synthesis of ketoprofen

Bennetau,Krempp,Dunogues

, p. 77 - 83 (1994)

A simple and convenient synthesis of 3-benzoylcyclohexanone, a ketoprofen precursor, is proposed. It consists of the preparation of 5-trimethylsilyl-3-cyclohexenone via disilylation of anisole followed by hydrolysis and subsequent regiospecific benzoylati

Benzothiazolines as radical transfer reagents: Hydroalkylation and hydroacylation of alkenes by radical generation under photoirradiation conditions

Uchikura, Tatsuhiro,Moriyama, Kaworuko,Toda, Mitsuhiro,Mouri, Toshiki,Ibá?ez, Ignacio,Akiyama, Takahiko

, p. 11171 - 11174 (2019/09/30)

Novel radical transfer reagents under photoirradiation conditions were developed by the use of benzothiazoline derivatives. These reagents enabled both hydroalkylation and hydroacylation of alkenes under neutral conditions at ambient temperature without a

Direct Aldehyde Csp2?H Functionalization through Visible-Light-Mediated Photoredox Catalysis

Vu, Minh Duy,Das, Mrinmoy,Liu, Xue-Wei

supporting information, p. 15899 - 15902 (2017/11/15)

The development of methods for carbon–carbon bond formation under benign conditions is an ongoing challenge for synthetic chemists. In recent years there has been considerable interest in using selective C?H activation as a direct route for generating rea

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