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52045-42-8

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52045-42-8 Usage

General Description

4-fluoro-2-methyl-1-indanone is a chemical compound with the molecular formula C10H9FO. It is a derivative of indanone, which is a bicyclic aromatic ketone. 4-fluoro-2-methyl-1-indanone is used in organic synthesis and pharmaceutical research, and it is considered as a building block for the synthesis of various pharmaceuticals. It is also used as a precursor in the manufacturing of other chemicals. 4-fluoro-2-methyl-1-indanone has several potential applications in the pharmaceutical and chemical industries due to its versatile reactivity and functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 52045-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,4 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52045-42:
(7*5)+(6*2)+(5*0)+(4*4)+(3*5)+(2*4)+(1*2)=88
88 % 10 = 8
So 52045-42-8 is a valid CAS Registry Number.

52045-42-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluoro-2-methyl-2,3-dihydroinden-1-one

1.2 Other means of identification

Product number -
Other names 4-Fluoro-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:52045-42-8 SDS

52045-42-8Downstream Products

52045-42-8Relevant articles and documents

Nickel-Catalyzed Domino Heck-Type Reactions Using Methyl Esters as Cross-Coupling Electrophiles

Zheng, Yan-Long,Newman, Stephen G.

supporting information, p. 18159 - 18164 (2019/11/13)

While esters are frequently used as traditional electrophiles in substitution chemistry, their application in cross-coupling chemistry is still in its infancy. This work demonstrates that methyl esters can be used as coupling electrophiles in Ni-catalyzed Heck-type reactions through the challenging cleavage of the C(acyl)?O bond under relatively mild reaction conditions at either 80 or 100 °C. With the σ-NiII intermediate generated from the insertion of acyl NiII species into the tethered C=C bond, carbonyl-retentive products were formed by domino Heck/Suzuki–Miyaura coupling and Heck/reduction pathways when organoboron and mild hydride nucleophiles are used.

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