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15507-35-4 Usage

Chemical Class

Benzyl derivatives
A class of chemical compounds that includes 1-cyclopentenyl phenylmethane.

Synthesis of pharmaceutical compounds

Commonly used as an intermediate or building block in the creation of various pharmaceutical products.

Medicinal properties

Has been studied for its potential to be used in medicine due to its unique chemical structure and properties.

Cancer cell growth inhibition

Investigated for its ability to inhibit the growth of cancer cells, making it a potential candidate for future cancer therapy.

Anti-inflammatory properties

Helps reduce inflammation, which can be beneficial in treating various inflammatory conditions and may make it a valuable ingredient in skincare products.

Applications in medicine, skincare, and cosmetics

Due to its wide range of potential applications, 1-cyclopentenyl phenylmethane can be used in the development of new drugs, skincare products, and cosmetics.

Check Digit Verification of cas no

The CAS Registry Mumber 15507-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,0 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15507-35:
(7*1)+(6*5)+(5*5)+(4*0)+(3*7)+(2*3)+(1*5)=94
94 % 10 = 4
So 15507-35-4 is a valid CAS Registry Number.

InChI:InChI=1/C12H14/c1-2-6-11(7-3-1)10-12-8-4-5-9-12/h1-3,6-8H,4-5,9-10H2

15507-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-CYCLOPENTENYL PHENYLMETHANE

1.2 Other means of identification

Product number	-
Other names	1-Cyclopentenyl phentlmehane

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:15507-35-4 SDS

15507-35-4Upstream product

15507-35-4Downstream Products

15507-35-4Relevant articles and documents

Grubbs Metathesis Enabled by a Light-Driven gem-Hydrogenation of Internal Alkynes

Biberger, Tobias,Fürstner, Alois,Zachmann, Raphael J.

supporting information, p. 18423 - 18429 (2020/08/25)

[(NHC)(cymene)RuCl2] (NHC=N-heterocyclic carbene) complexes instigate a light-driven gem-hydrogenation of internal alkynes with concomitant formation of discrete Grubbs-type ruthenium carbene species. This unorthodox reactivity mode is harnessed in the form of a “hydrogenative metathesis” reaction, which converts an enyne substrate into a cyclic alkene. The intervention of ruthenium carbenes formed in the actual gem-hydrogenation step was proven by the isolation and crystallographic characterization of a rather unusual representative of this series carrying an unconfined alkyl group on a disubstituted carbene center.

Alder-ene reaction of aryne with olefins

Chen, Zhao,Liang, Jinhua,Yin, Jun,Yu, Guang-Ao,Liu, Sheng Hua

supporting information, p. 5785 - 5787 (2013/10/01)

A novel intermolecular Alder-ene reaction based on aryne and olefins was developed. We performed this transformation under mild conditions such as at room temperature, and this reaction displayed high selectivity and good yields only in the presence of CsF. Hence, the intermolecular Alder-ene reaction of aryne with olefins provides an effective route to synthesize derivatives of olefins.

Ruthenium complex-catalyzed novel transformation of alkyl formates

Kondo, Teruyuki,Kajiya, Satoshi,Tantayanon, Supawan,Watanabe, Yoshihisa

, p. 83 - 92 (2007/10/02)

The following ruthenium-catalyzed novel transformations of alkyl formates have been developed: (1) selective decarbonylation of alkyl formates to the corresponding alcohols; (2) alkylation of arenes and alkenes using alkyl formates as an alkylating reagent via decarboxylation.Also the ruthenium-catalyzed addition of alcohols to alkenes has been developed as an appendant reaction, providing an effective method for the protection of alcohols.Keywords: Ruthenium; Catalysis; Alkyl; Arene; Alkene; Alcohol

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15507-35-4