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2-Cyclohepten-1-ylacetate is a chemical compound with the molecular formula C9H12O2. It is a derivative of cycloheptane, a seven-membered cyclic hydrocarbon, and acetic acid. 2-Cyclohepten-1-ylacetate features a cycloheptene ring with a double bond between the second and third carbon atoms, and an acetate group attached to the first carbon atom. The acetate group consists of a methyl group (CH3) and a carboxyl group (COOH), which is esterified to the cycloheptene ring. 2-Cyclohepten-1-ylacetate is an organic compound that can be used in various chemical reactions and synthesis processes, particularly in the pharmaceutical and chemical industries. Its unique structure and properties make it a valuable intermediate in the preparation of various organic compounds and pharmaceuticals.

826-13-1

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826-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 826-13-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 826-13:
(5*8)+(4*2)+(3*6)+(2*1)+(1*3)=71
71 % 10 = 1
So 826-13-1 is a valid CAS Registry Number.

826-13-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(cyclohepten-1-yl)acetate

1.2 Other means of identification

Product number -
Other names (?A'A A'A currency)-3-Acetoxycycloheptene

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:826-13-1 SDS

826-13-1Relevant academic research and scientific papers

PALLADIUM-CATALYZED ALLYLIC OXIDATION OF OLEFINS BY t-BUTYL HYDROPEROXIDE AND TELLURIUM(IV) OXIDE

Uemura, Sakae,Fukuzawa, Shin-ichi,Toshimitsu, Akio,Okano, Masaya

, p. 87 - 90 (2007/10/02)

Treatment of several cyclic olefins, β-pinene, allylbenzene and estragole with palladium(II) salt in acetic acid in the presence of t-butyl hydroperoxide and tellurium(IV) oxide afforded mainly the corresponding allylic acetates.The reaction proceeded catalytically with palladium(II) salt, t-BuOOH working as a reoxidazing agent.

OAc AS A HOMOGENEOUS CATALYST FOR SELECTIVE ENONE FORMATION BY ALLYLIC OXIDATION OF OLEFINS

Uemura, Sakae,Patil, Suresh R.

, p. 4353 - 4356 (2007/10/02)

Treatment of several cyclic olefins and allylbenzene with a catalytic amount of OAc in acetic acid in the presence of t-butyl hydroperoxide affords the corresponding α,β-unsaturated carbonyl compounds(enones) highly selectively via an ionic pathway.

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