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7111-29-7

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7111-29-7 Usage

General Description

"(1R-cis)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-yl acetate, also known as cis-jasmone, is a natural organic compound that belongs to the class of cyclohexenones. It can be found in jasmine and other plants, where it contributes to their characteristic fragrance. Cis-jasmone is used in perfumery and flavoring due to its sweet, floral, and fruity odor. It also has potential applications in agriculture, as it has been shown to affect plant growth and development, as well as have repellent effects on certain insects. In addition, cis-jasmone has demonstrated bioactivity in laboratory studies, showing potential as an anti-cancer and anti-inflammatory agent."

Check Digit Verification of cas no

The CAS Registry Mumber 7111-29-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,1 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7111-29:
(6*7)+(5*1)+(4*1)+(3*1)+(2*2)+(1*9)=67
67 % 10 = 7
So 7111-29-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O2/c1-8(2)11-6-5-9(3)12(7-11)14-10(4)13/h5,11-12H,1,6-7H2,2-4H3/t11-,12-/m0/s1

7111-29-7SDS

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 (1R-cis)-2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-ol acetate

1.2 Other means of identification

Product number -
Other names (-)-cis-carvyl acetate

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:7111-29-7 SDS

7111-29-7Relevant articles and documents

Formyloxyacetoxyphenylmethane and 1,1-diacylals as versatile O-formylating and O-acylating reagents for alcohols

Chapman, Robert S.L.,Francis, Molly,Lawrence, Ruth,Tibbetts, Joshua D.,Bull, Steven D.

, p. 6442 - 6452 (2018/10/02)

Formyloxyacetoxyphenylmethane, symmetric 1,1-diacylals and mixed 1-pivaloxy-1-acyloxy-1-phenylmethanes have been used as moisture stable O-formylating and O-acylating reagents for primary and secondary alcohols, allylic alcohols and phenols under solvent/catalyst free conditions to afford their corresponding esters in good yield.

Titanium carbenoid-mediated cyclopropanation of allylic alcohols: Selectivity and mechanism

Durán-Pe?a,Botubol-Ares,Hanson,Hernández-Galán,Collado

, p. 6325 - 6332 (2015/06/08)

A new method for the chemo- and stereoselective conversion of allylic alcohols into the corresponding cyclopropane derivatives has been developed. The cyclopropanation reaction was carried out with an unprecedented titanium carbenoid generated in situ from Nugent's reagent, manganese and methylene diiodide. The reaction involving the participation of an allylic hydroxyl group, proceeded with conservation of the alkene geometry and in a high diastereomeric excess. The scope, limitations and mechanism of this metal-catalysed reaction are discussed. This journal is

The claisen rearrangement in synthesis: Acceleration of the johnson orthoester protocol en route to bicyclic lactones

Jones, Graham B.,Huber, Robert S.,Chau, Sotheary

, p. 369 - 380 (2007/10/02)

Catalysis of the Claisen orthoester rearrangement of triethyl orthoacetate and a number of 2-cycloalken-1-ols has been achieved using acidic catalysis and brief microwave thermolysis in DMF. Unlike conventional methods of thermolysis, very high yields of rearranged products are typically obtained in less than ten minutes, and the Claisen products themselves require no further purification. The synthetic utility of the products so obtained is demonstrated in a general synthesis of functionalized bicyclic lactones.

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