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1-Indanone, 3-methyl-6-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71823-53-5

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71823-53-5 Usage

General Description

1-Indanone, 3-methyl-6-phenyl- is a chemical compound with the molecular formula C15H14O. It is a fragrant organic compound with a distinct odor and is commonly used in the synthesis of various pharmaceuticals and fragrances. 1-Indanone, 3-methyl-6-phenyl- is also used as a precursor in the production of indacaterol, a drug used to treat chronic obstructive pulmonary disease. It is a white crystalline solid at room temperature and is insoluble in water but soluble in organic solvents. 1-Indanone, 3-methyl-6-phenyl- is considered to be a valuable building block in the production of fine chemicals and can be used in the synthesis of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 71823-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,2 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71823-53:
(7*7)+(6*1)+(5*8)+(4*2)+(3*3)+(2*5)+(1*3)=125
125 % 10 = 5
So 71823-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O/c1-11-9-16(17)15-10-13(7-8-14(11)15)12-5-3-2-4-6-12/h2-8,10-11H,9H2,1H3

71823-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 1-Indanone,3-methyl-6-phenyl

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:71823-53-5 SDS

71823-53-5Downstream Products

71823-53-5Relevant academic research and scientific papers

Asymmetric Induction in Hydroacylation by Cooperative Iminium Ion-Transition-Metal Catalysis

Rastelli, Ettore J.,Truong, Ngoc T.,Coltart, Don M.

supporting information, p. 5588 - 5591 (2016/11/17)

A new strategy for the rhodium-catalyzed enantioselective hydroacylation is described. This has been achieved through the merger of iminium ion catalysis and transition-metal catalysis such that asymmetric induction derives from a readily accessible, inexpensive chiral nonracemic secondary amine catalyst rather than a chiral nonracemic phosphine as is typical of conventional asymmetric hydroacylation methods.

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