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(1-chlorocyclohexyl)(phenyl)methanone, also known as PCPM, is an organic compound with the molecular formula C13H15ClO. It is a ketone, characterized by a carbonyl group attached to two alkyl groups. PCPM is a colorless liquid with a molecular weight of 216.71 g/mol. Due to its potentially hazardous nature, it is important to handle PCPM with care.

1135-71-3

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1135-71-3 Usage

Uses

Used in Pharmaceutical Research:
PCPM is utilized as a precursor in the synthesis of various pharmaceuticals and other organic compounds. Its unique structure and reactivity make it a valuable component in the development of new drugs and medicinal agents.
Used in Chemical Production:
PCPM serves as an intermediate in the production of other chemicals. Its versatility in chemical reactions allows it to be a key component in the synthesis of a wide range of chemical products.
Used in Research and Development:
Due to its potential applications in various fields, PCPM is used in research and development to explore its properties and discover new uses. Its reactivity and structural features make it an interesting subject for scientific investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 1135-71-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1135-71:
(6*1)+(5*1)+(4*3)+(3*5)+(2*7)+(1*1)=53
53 % 10 = 3
So 1135-71-3 is a valid CAS Registry Number.

1135-71-3SDS

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 (1-chlorocyclohexyl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names -

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:1135-71-3 SDS

1135-71-3Relevant academic research and scientific papers

Preparation method of photoinitiator

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, (2021/10/13)

The invention discloses a preparation method of a photoinitiator. The preparation method comprises the following steps: acid chloride required for Fries reaction, aluminum trichloride and a solvent are mixed and then subjected to a Fourier reaction with benzene. Fries reaction intermediate purification method The Fourier reaction intermediate is mixed with chlorine for chlorination reaction, and the product of the chlorination reaction is subjected to gas-liquid separation to separate the gas. Reaction Section Step and The product purification step results in a photoinitiator finished product. To the technical scheme of the invention, the advantages of the traditional process of producing the photoinitiator are combined with the characteristics of the microchannel reactor to realize continuous preparation, the productivity can be improved, the production risk is reduced, the manpower and equipment investment are reduced, and the cost is further reduced.

Method for preparing alpha-hydroxy ketone photoinitiator in microreactor

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Paragraph 0024; 0030, (2020/05/05)

The invention relates to a method for preparing an alpha-hydroxy ketone photoinitiator in a microreactor. The method comprises the following steps: introducing chlorine into isobutyryl benzene servingas a raw material to obtain an intermediate chloroisobutyryl chloride, and carrying out alkaline hydrolysis on the intermediate under the action of an aqueous sodium hydroxide solution to obtain thealpha-hydroxy ketone photoinitiator. The preparation method of the alpha-hydroxy ketone photoinitiator has the advantages of high operation safety, high selectivity, small reaction volume, short reaction time, low equipment corrosion, low energy consumption and environment friendliness, and is a process method suitable for industrial production.

Synthesis method of photoinitiator 1-hydroxycyclohexyl phenyl ketone

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Paragraph 0023-0028, (2020/12/05)

The invention aims to solve the technical problems of an existing alpha-hydroxycyclohexyl phenyl ketone synthesis method, provides a synthesis method of a photoinitiator 1-hydroxycyclohexyl phenyl ketone, and belongs to the technical field of chemical synthesis. The synthesis method comprises the following steps: (1) reacting a halogenated benzene with magnesium particles to prepare a Grignard reagent, dropwise adding cyclohexylcarbonitrile into the prepared Grignard reagent, and after the reaction is completed, hydrolyzing to generate cyclohexyl phenyl ketone; and (2) reacting cyclohexyl phenyl ketone with chlorine to obtain 1-chlorocyclohexyl phenyl ketone, and carrying out a hydrolysis reaction on the 1-chlorocyclohexyl phenyl ketone and a sodium hydroxide aqueous solution under the action of a catalyst to obtain 1-hydroxycyclohexyl phenyl ketone. The method is simple in synthesis process, high in yield and suitable for industrial production.

Synthetic method of photoinitiator 1-hydroxycyclohexyl phenyl ketone

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, (2019/08/12)

The invention discloses a synthetic method of a photoinitiator 1-hydroxycyclohexyl phenyl ketone. The synthetic method comprises the following steps: enabling cyclohexanecarboxylic acid chloride and benzene to be subjected to electrophilic substitution reaction under the catalysis of Lewis acid to obtain cyclohexyl phenyl ketone; enabling the cyclohexyl phenyl ketone to react with hydrogen peroxide and a hydrochloric acid solution under the action of a molecular sieve catalyst to obtain 1-chlorocyclohexyl phenyl ketone; and enabling the 1-chlorocyclohexyl phenyl ketone and a sodium hydroxide aqueous solution to be subjected to hydrolysis reaction under the action of the catalyst to obtain the 1-hydroxycyclohexyl phenyl ketone. The synthetic method disclosed by the invention has the advantages that the raw materials are cheap, easily-available, safe and environmentally friendly; hydrogen chloride produced by electrophilic substitution reaction of acyl chloride under the catalysis of Lewis acid is fully utilized and recycled, thereby reducing the discharge of waste acid water and being friendly to the environment; and selective chlorination and hydrolysis are completed in the same reactor, the operation is simple, the loss is less, and the yield is high.

PROCESS FOR THE PREPARATION OF AROMATIC ALPHA-HYDROXY KETONES

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, (2011/04/18)

Process for the preparation of aromatic alpha-hydroxyketones (aromatic α-hydroxyketones) that does not require the use of chlorine, sulfuryl chloride or bromine and comprises the halogenation of an intermediate aromatic ketone with a hydrogen halide in the presence of an oxidising compound.

PROCESS FOR THE PREPARATION OF AROMATIC ALPHA-HYDROXY KETONES

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Page/Page column 18, (2010/01/29)

Process for the preparation of aromatic alpha-hydroxyketones (aromatic α- hydroxyketones) that does not require the use of chlorine, sulfuryl chloride or bromine and comprises the halogenation of an intermediate aromatic ketone with a hydrogen halide in the presence of an oxidising compound.

1,2-Addition of α,α,α-trichlorotoluene to ketones via a Mg Barbier reaction in DMF: New route to cycloalk-1-en-1-yl and alk-1-en-1-yl phenyl ketones

Aaziz, Akima,Oudeyer, Sylvain,Leonel, Eric,Paugam, Jean Paul,Nedelec, Jean-Yves

, p. 1147 - 1154 (2008/02/01)

The reductive cyclocondensation of α,α,α-trichlorotoluene to enolisable ketones enables the preparation of (cyclo)alken-1-en-1-yl phenyl ketones via the formation of an intermediate chlorooxirane. Copyright Taylor & Francis Group, LLC.

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