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176088-59-8

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176088-59-8 Usage

General Description

6-Bromo-2-methyl-1-indanone is a chemical compound with the molecular formula C10H9BrO. It belongs to the group of compounds known as indanones, which are cyclic ketones with a structure based on the indane skeleton. As its name suggests, it has a bromine atom at position 6 and a methyl group at position 2 of the indanone ring. Its molecular structure is characterized by the presence of a ketone functional group which is the oxygen atom double bonded to the carbon atom, resulting in its reactivity. This chemical is commonly used in scientific research and can be used as an intermediate in organic synthesis. Given the specificity of its structure, it has potential applications in pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 176088-59-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,0,8 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 176088-59:
(8*1)+(7*7)+(6*6)+(5*0)+(4*8)+(3*8)+(2*5)+(1*9)=168
168 % 10 = 8
So 176088-59-8 is a valid CAS Registry Number.

176088-59-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-2-methyl-2,3-dihydroinden-1-one

1.2 Other means of identification

Product number -
Other names 6-Bromo-2-methyl-2,3-dihydro-1H-inden-1-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:176088-59-8 SDS

176088-59-8Upstream product

176088-59-8Downstream Products

176088-59-8Relevant articles and documents

Preparation of acrylophenones and 2-alkyl indanones utilizing hexamethylenetetramine as an inexpensive Mannich reagent

Bhattacharya, Apurba,Segmuller, Brigitte,Ybarra, Arnold

, p. 1775 - 1784 (1996)

Hexamethylenetetramine/acetic anhydride-promoted α-methylenation of aryl alkyl ketones followed by acid-catalyzed cyclization of the resulting acrylophenones produce 2-alkyl indanones in excellent yields.

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