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2-Cyclopenten-1-one, 5,5-dimethyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75107-76-5

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75107-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75107-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,0 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75107-76:
(7*7)+(6*5)+(5*1)+(4*0)+(3*7)+(2*7)+(1*6)=125
125 % 10 = 5
So 75107-76-5 is a valid CAS Registry Number.

75107-76-5SDS

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 5,5-dimethyl-2-phenylcyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Cyclopenten-1-one,5,5-dimethyl-2-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:75107-76-5 SDS

75107-76-5Relevant academic research and scientific papers

Solvent-controlled photocatalytic divergent cyclization of alkynyl aldehydes: access to cyclopentenones and dihydropyranols

Feng, Jian,Kong, Lichun,Xue, Xiao-Song,Zhang, Fang,Zhang, Junhua,Zheng, Hanliang,Zhu, Gangguo,Zhu, Haiqian

, p. 11420 - 11426 (2021/09/07)

Divergent synthesis is a powerful strategy for the fast assembly of different molecular scaffolds from identical starting materials. We describe here a solvent-controlled photocatalytic divergent cyclization of alkynyl aldehydes with sulfonyl chlorides for the direct construction of highly functionalized cyclopentenones and dihydropyranols that widely exist in bioactive molecules and natural products. Density functional theory calculations suggest that a uniqueN,N-dimethylacetamide-assisted 1,2-hydrogen transfer of alkoxy radicals is responsible for the cyclopentenone formation, whereas a C-C cleavage accounts for the selective production of dihydropyranols in acetonitrile and water at 50 °C. Given the simple and mild reaction conditions, excellent functional group compatibility, forming up to four chemical bonds, and tunable selectivity, it may find wide applications in synthetic chemistry.

Diaryl-2-(5H)-furanones as Cox-2 inhibitors

-

, (2008/06/13)

The invention encompasses the novel compound of Formula (I) as well as a method of treating cyclooxygenase-2 mediated diseases comprising administration to a patient in need of such treatment of a non-toxic therapeutically effective amount of a compound of Formula (I). The invention also encompasses certain pharmaceutical compositions for treatment of cyclooxygenase-2 mediated diseases comprising compounds of Formula (I).

A DIRECT THREE-CARBON ANNELATION TO CYCLOPENTENONE DERIVATIVES

Prempree, P.,Siwapinyoyos T.,Thebtaranonth, C.,Thebtaranonth, Y.

, p. 1169 - 1172 (2007/10/02)

Cyclopentenone derivatives were prepared by three-carbon alkylation followed by cyclisation of the ester.

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