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68293-31-2

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68293-31-2 Usage

General Description

7-Hydroxy-6-Methyl-1-indanone is a chemical compound that belongs to the class of indanone derivatives. It is a yellow crystalline powder with a melting point of 119-121°C and has a molecular formula C10H10O2. 7-Hydroxy-6-Methyl-1-indanone is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. It has also been studied for its potential biological activities, including its antioxidant and anti-inflammatory properties. Additionally, 7-Hydroxy-6-Methyl-1-indanone has been investigated for its potential use in the development of new drugs due to its unique chemical structure and potential pharmacological effects.

Check Digit Verification of cas no

The CAS Registry Mumber 68293-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,9 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 68293-31:
(7*6)+(6*8)+(5*2)+(4*9)+(3*3)+(2*3)+(1*1)=152
152 % 10 = 2
So 68293-31-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O2/c1-6-2-3-7-4-5-8(11)9(7)10(6)12/h2-3,12H,4-5H2,1H3

68293-31-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-hydroxy-6-methyl-2,3-dihydroinden-1-one

1.2 Other means of identification

Product number -
Other names 6-Methyl-7-hydroxy-1-indanon

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:68293-31-2 SDS

68293-31-2Relevant articles and documents

Gold catalysis: Efficient synthesis and structural assignment of jungianol and epi-jungianol

Hashmi, A. Stephen K.,Ding, Li,Bats, Jan W.,Fischer, Peter,Frey, Wolfgang

, p. 4339 - 4345 (2003)

Starting from 2-methylfuran and crotonaldehyde, both jungianol and epijungianol were prepared by a six-step sequence including a gold-catalyzed arene synthesis and a photochemical SN2-like reduction with lithium aluminum hydride. Not a single p

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