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2H-Azepin-2-one,hexahydro-7-isopropyl-(6CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102539-72-0

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102539-72-0 Usage

Chemical compound

2H-Azepin-2-one, hexahydro-7-isopropyl

Commonly known as

Cyclooctanone

Properties

Colorless liquid with a strong and pungent odor

Solubility

Slightly soluble in water, highly soluble in organic solvents

Uses

Building block in the synthesis of pharmaceuticals and fine chemicals

Caution

Handle with care due to potential health risks if not used properly

Check Digit Verification of cas no

The CAS Registry Mumber 102539-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,3 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102539-72:
(8*1)+(7*0)+(6*2)+(5*5)+(4*3)+(3*9)+(2*7)+(1*2)=100
100 % 10 = 0
So 102539-72-0 is a valid CAS Registry Number.

102539-72-0SDS

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 7-isopropyl-hexahydro-azepin-2-one

1.2 Other means of identification

Product number -
Other names (R)-7-Isopropyl-azepan-2-one

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:102539-72-0 SDS

102539-72-0Downstream Products

102539-72-0Relevant academic research and scientific papers

A convenient synthesis of medium-sized lactams through RCM reaction of oxyoxazolidinones

Kamimura, Akio,Tanaka, Keiichi,Hayashi, Takahiro,Omata, Yoji

, p. 3625 - 3627 (2007/10/03)

Oxyoxazolidinones, which are prepared from secondary O-acylmandelamides by treatment with TBSOTf, underwent the RCM reaction in the presence of Grubbs catalyst to give oxazoloazepines or oxazoloazecines, which were readily converted into N-unsubstituted seven-membered or eight-membered lactams by the reductive treatment.

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