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Undecan-1-en-3-yl acetate, also known as 3-undecenyl acetate, is an organic compound with the chemical formula C13H24O2. It is a colorless to pale yellow liquid with a fruity, green, and slightly fatty odor. This ester is commonly used as a fragrance ingredient in various personal care products, such as perfumes, soaps, and lotions, due to its pleasant scent. It is also found in some natural essential oils, like orange and lemon, contributing to their characteristic aromas. The compound is synthesized by the esterification of undec-1-en-3-ol with acetic acid, and it is considered safe for use in fragrances at the concentrations typically employed.

94088-25-2

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94088-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94088-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,8 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94088-25:
(7*9)+(6*4)+(5*0)+(4*8)+(3*8)+(2*2)+(1*5)=152
152 % 10 = 2
So 94088-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H24O2/c1-4-6-7-8-9-10-11-13(5-2)15-12(3)14/h5,13H,2,4,6-11H2,1,3H3

94088-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name undec-1-en-3-yl acetate

1.2 Other means of identification

Product number -
Other names EINECS 302-023-4

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:94088-25-2 SDS

94088-25-2Downstream Products

94088-25-2Relevant academic research and scientific papers

A chiral Lewis acid strategy for enantioselective allylic C-H oxidation

Covell, Dustin J.,White, M. Christina

supporting information; experimental part, p. 6448 - 6451 (2009/03/11)

(Chemical Equation Presented) Skip the chiral ligand: A chiral Lewis acid strategy for effecting asymmetric induction in oxidative systems not amenable to strongly binding chiral ligands is disclosed and its mechanism investigated. The highest levels of enantioselectivity for allylic C-H oxidation of terminal olefins is reported (see scheme; BQ=1,4-benzoquinone, LA=chiral Lewis acid).

Serial ligand catalysis: A highly selective allylic C-H oxidation

Chen, Mark S.,Prabagaran, Narayanasamy,Labenz, Nathan A.,White, M. Christina

, p. 6970 - 6971 (2007/10/03)

We are reporting a mild, chemo-, and highly regioselective Pd(II)-catalyzed allylic oxidation of α-olefins to furnish branched allylic esters that proceeds via a novel serial ligand catalysis mechanism in which two different ligands (i.e., vinyl sulfoxide 2 and BQ) interact sequentially with the metal to promote distinct steps of the catalytic cycle (i.e., C-H cleavage and π-allyl functionalization, respectively). Copyright

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