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Cyclopentene-1-methanol is an organic compound with the chemical formula C6H12O. It is a cyclic alkene with a hydroxyl group attached to the first carbon atom of the cyclopentane ring. This molecule is characterized by its five-membered carbon ring structure, with one double bond between two of the carbon atoms, and a hydroxyl group (-OH) attached to one of the carbons. Cyclopentene-1-methanol is a colorless liquid with a pungent odor and is soluble in water. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactive nature, it is important to handle Cyclopentene-1-methanol with care, as it can undergo various chemical reactions such as oxidation, reduction, and substitution.

1120-80-5

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1120-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1120-80-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1120-80:
(6*1)+(5*1)+(4*2)+(3*0)+(2*8)+(1*0)=35
35 % 10 = 5
So 1120-80-5 is a valid CAS Registry Number.

1120-80-5SDS

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 cyclopenten-1-ylmethanol

1.2 Other means of identification

Product number -
Other names 1-Cyclopentene-1-methanol

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:1120-80-5 SDS

1120-80-5Relevant academic research and scientific papers

Reduction of carboxylic acids using esters of benzotriazole as high-reactivity intermediates

Morales-Serna, Jose Antonio,Garcia-Rios, Erendira,Bernal, Jorge,Paleo, Ehecatl,Gavino, Ruben,Cardenas, Jorge

scheme or table, p. 1375 - 1382 (2011/06/19)

Herein, we describe a simple and practical protocol for the reduction of carboxylic acids via the in situ formation of hydroxybenzotriazole esters followed by reaction with sodium borohydride to give the corresponding alcohols. The reaction proceeds with excellent yields in the presence of water. Georg Thieme Verlag Stuttgart - New York.

Studies on the Autoxidation of Some Monocyclic Olefins

Blau, K.,Mueller, U.,Pritzkow, W.,Schmidt-Renner, W.,Sedshaw, Z.

, p. 915 - 932 (2007/10/02)

The autoxidations of cyclopentene, cyclohexene, cycloheptene, cyclooctene, cycloocta-1,5-diene, 1-methylcyclopentene, 1-methylcyclohexene, 1-methylcycloheptene, 1-methylcyclooctene, methylene cyclopentene, and methylene cyclohexene with pure oxygen under normal pressure were studied.The epoxides formed were determined gaschromatographically.In most cases also the products of allylic oxidation were analyzed and their structures elucidated after reduction to the corresponding allyl alcohols.The portions of high boiling or polymeric products which could not be detected gaschromatographically and also the real yields of epoxides were determined by balance experiments in the presence of inert internal standards.

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