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62907-55-5

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62907-55-5 Usage

Structure

Bicyclic aromatic ketone

Usage

Building block in the synthesis of pharmaceuticals and organic compounds

Odor

Strong aromatic and musky

Application

Production of perfumes and fragrances

Potential properties

Antimicrobial and anti-inflammatory

Importance

Valuable in medicinal chemistry and chemical industry due to its unique structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 62907-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,0 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62907-55:
(7*6)+(6*2)+(5*9)+(4*0)+(3*7)+(2*5)+(1*5)=135
135 % 10 = 5
So 62907-55-5 is a valid CAS Registry Number.

62907-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2-phenyl-2,3-dihydroinden-1-one

1.2 Other means of identification

Product number -
Other names 3-Methyl-2-phenyl-indan-1-on

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:62907-55-5 SDS

62907-55-5Relevant articles and documents

Cobalt-Catalyzed Enantio- and Diastereoselective Intramolecular Hydroacylation of Trisubstituted Alkenes

Yang, Junfeng,Rérat, Alice,Lim, Yang Jie,Gosmini, Corinne,Yoshikai, Naohiko

supporting information, p. 2449 - 2453 (2017/02/23)

Enantio- and diastereoselective synthesis of trans-2,3-disubstituted indanones is achieved by intramolecular hydroacylation of 2-alkenylbenzaldehydes bearing trisubstituted alkenyl groups under cobalt-chiral diphosphine catalysis. Notably, a high level of enantioselectivity is induced regardless of the stereochemistry (E/Z ratio) of the alkenyl group of the starting material. Deuterium-labeling experiments shed light on the productive reaction pathways of the E- and Z-isomers.

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