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2-[4-(isopropyl)phenyl]cyclohexan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84604-97-7

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84604-97-7 Usage

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Chemical compound

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Complex molecular structure

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Classified as a cyclohexanone

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Contains isopropyl and phenyl groups

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Versatile building block for synthesis of other organic compounds

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Widely used in chemical industry

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Used as a reagent for chemical reactions

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Used as a precursor for fine chemicals production

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Important component in synthesis of organic compounds

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Name 2-[4-(isopropyl)phenyl]cyclohexan-1-one

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Also known as IPC

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Commonly used in production of pharmaceuticals, dyes, and perfumes

Check Digit Verification of cas no

The CAS Registry Mumber 84604-97-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,0 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84604-97:
(7*8)+(6*4)+(5*6)+(4*0)+(3*4)+(2*9)+(1*7)=147
147 % 10 = 7
So 84604-97-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O/c1-11(2)12-7-9-13(10-8-12)14-5-3-4-6-15(14)16/h7-11,14H,3-6H2,1-2H3

84604-97-7SDS

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 2-(4-propan-2-ylphenyl)cyclohexan-1-one

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:84604-97-7 SDS

84604-97-7Downstream Products

84604-97-7Relevant academic research and scientific papers

Transition-Metal-Free Site-Selective γ-C(sp2)-H Monoiodination of Arenes Directed by an Aliphatic Keto Group

Bian, Hong-Li,Tang, Shi-Zhong,Chen, Meng-En,Zhang, Xiao-Ming,Lv, Jian-Wei,Chen, Xiao-Wei,Qi, Feng-Ming,Chen, Shi-Wu,Zhang, Fu-Min

supporting information, p. 5314 - 5319 (2020/07/08)

A general γ-C(sp2)-H iodination method directed by an aliphatic keto group has been developed under transition-metal-free conditions for the first time, generating iodoarenes in good to excellent yields with excellent site selectivity. This protocol features a wide range of aryl-substituted ketones, short reaction times, mild reaction conditions, and scalable synthetic procedures. A possible reaction mechanism was also proposed based on several control experiments.

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