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2114-32-1

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2114-32-1 Usage

Common uses

Flavoring agent and fragrance ingredient

Classification

Ester (formed by the reaction of an alcohol and a carboxylic acid)

Found in

Perfumes, colognes, scented household items

Odor

Sweet, fruity with floral undertones

Used in

Consumer goods for adding pleasant scent

Industry

Food industry (baked goods and confectionery items)

Safety

Can be irritating to skin and eyes

Handling

Should be used in accordance with safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 2114-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2114-32:
(6*2)+(5*1)+(4*1)+(3*4)+(2*3)+(1*2)=41
41 % 10 = 1
So 2114-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O2/c1-3-11(13-9(2)12)10-7-5-4-6-8-10/h10-11H,3-8H2,1-2H3

2114-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexylpropyl acetate

1.2 Other means of identification

Product number -
Other names <1-Acetoxy-propyl>-cyclohexan

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:2114-32-1 SDS

2114-32-1Downstream Products

2114-32-1Relevant articles and documents

Planar- and central-chiral N,O-[2.2]paracyclophane ligands: Non-linear-like effects and activity

Lauterwasser, Frank,Vanderheiden, Sylvia,Braese, Stefan

, p. 443 - 448 (2006)

The non-linear-like effect (NLLE), activity, temperature dependence, and kinetics of hydroxy-[2.2]paracyclophane ketimine ligands have been investigated with the 1,2-addition reaction of diethylzinc to cyclohexanecarbaldehyde. A linear correlation between the enantiomeric excess of AHPC ketimine ligands bearing a phenylethyl side group and the product was observed with 0.5 mol% of catalyst loading. On increasing the catalyst loading to 4 mol%, a precipitate of the inactive heterochiral species was formed and resulted in a positive non-linear-like effect. The enantiomeric ratio was found to have linear temperature dependence.

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