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7063-68-5

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7063-68-5 Usage

General Description

CYCLOPENTYL 2-METHOXYPHENYL KETONE, also known as 2-Methoxy-4'-cyclopentylacetophenone, is an organic compound commonly used in the pharmaceutical and chemical industries. It is a ketone derivative, which means it contains a carbonyl group attached to two organic groups. The molecule consists of a cyclopentyl group attached to a 2-methoxyphenyl group by a carbonyl group. This chemical is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds due to its versatile reactivity and ability to form different chemical bonds. Additionally, it has been studied for its potential biological activities, such as anti-inflammatory and anti-cancer properties.

Check Digit Verification of cas no

The CAS Registry Mumber 7063-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7063-68:
(6*7)+(5*0)+(4*6)+(3*3)+(2*6)+(1*8)=95
95 % 10 = 5
So 7063-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C26H28N4O2S2/c1-4-29-23(28-12-8-9-17(2)15-28)20(18(3)21(14-27)24(29)31)13-22-25(32)30(26(33)34-22)16-19-10-6-5-7-11-19/h5-7,10-11,13,17H,4,8-9,12,15-16H2,1-3H3

7063-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopentyl-(2-methoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names CYCLOPENTYL 2-METHOXYPHENYL KETONE

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:7063-68-5 SDS

7063-68-5Relevant articles and documents

Direct catalytic asymmetric three-component Kabachnik-fields reaction

Cheng, Xu,Goddard, Richard,Buth, Gernot,List, Benjamin

supporting information; experimental part, p. 5079 - 5081 (2009/03/11)

(Chemical Equation Presented) As mimics of α-amino acids, α-amino phosphonates have great promise as antibacterial and anti-HIV agents as well as protease inhibitors. Racemic α-branched aldehydes react, in the presence the new chiral phosphoric acid catalyst 1, directly with p-anisidine (PMPNH2) and a phosphite to furnish β-branched α-amino phosphonates highly diastereoselectively and enantioselectively. Anth = anthracenyl.

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