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3-Cyclopentene-1-acetic acid is a chemical compound with the molecular formula C7H10O2. It is a derivative of cyclopentene, a five-membered cyclic hydrocarbon, with an acetic acid group attached to the first carbon atom. This organic compound is characterized by its unique structure, which combines the properties of both cyclopentene and acetic acid. It is a colorless liquid with a pungent odor and is soluble in organic solvents. 3-Cyclopentene-1-acetic acid has potential applications in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its reactive functional groups and unique cyclic structure.

767-03-3

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767-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 767-03-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 767-03:
(5*7)+(4*6)+(3*7)+(2*0)+(1*3)=83
83 % 10 = 3
So 767-03-3 is a valid CAS Registry Number.

767-03-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyclopent-3-en-1-ylacetic acid

1.2 Other means of identification

Product number -
Other names 3-Cyclopentene-1-acetic acid

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:767-03-3 SDS

767-03-3Relevant academic research and scientific papers

Preparation method and intermediate of fused tricyclic derivative

-

, (2020/08/27)

The invention provides a preparation method of a fused tricyclic derivative intermediate. The intermediate has a structure shown as a formula (4-7). The preparation method has the advantages of accessible raw materials and simple steps and is suitable for large-scale industrial production.

Acid-Catalyzed Hydrolysis of Bridged Bi- and Tricyclic Compounds. XXVI. The Mechanisms of Formation of the Hydration Products of 2-Norbornen-5-one

Lajunen, Martti,Lahti, Marjo,Heimo, Satu

, p. 771 - 776 (2007/10/02)

The acid-catalyzed hydration of 2-norbornen-5-one (1) in 5 mol dm-3 HClO4 at 358 K produces, according to GLC analyses, exo-5-hydroxy-2-norbornanone (2), 2-oxabicycloctan-3-one (3), which is in equilibrium with cis-3-hydroxycyclopentaneacetic acid (5), and 2-oxabicyclooctan-3-one (4).The former lactone (3) is unstable and rearranges slowly to the latter (4).The ketoalcohol (2) is formed via the slow protonation of norbornenone at C(3) and via subsequent hydration of the carbocation.The lactones are formed via complicated routes started by the protonation of norbornenone at C(2), and comprising 3- and 2-cyclopentaneacetic acid (7 and 9) as unstable intermediate products.

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