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Styralyl hexanoate, also known as 4-phenyl-2-butyl hexanoate, is an organic compound with the chemical formula C16H22O2. It is a colorless to pale yellow liquid with a fruity, floral, and slightly woody 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 and ability to enhance the aroma of other fragrance components. Styralyl hexanoate is also employed in the flavor industry, adding a sweet, fruity, and creamy taste to food products. It is synthesized through the esterification of styrallyl alcohol and hexanoic acid, and its safety profile is generally considered to be low risk for human health when used in appropriate concentrations.

3460-45-5

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3460-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3460-45-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3460-45:
(6*3)+(5*4)+(4*6)+(3*0)+(2*4)+(1*5)=75
75 % 10 = 5
So 3460-45-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O2/c1-3-4-6-11-14(15)16-12(2)13-9-7-5-8-10-13/h5,7-10,12H,3-4,6,11H2,1-2H3

3460-45-5SDS

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 1-phenylethyl hexanoate

1.2 Other means of identification

Product number -
Other names Hexanoic acid,1-phenylethyl ester

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:3460-45-5 SDS

3460-45-5Downstream Products

3460-45-5Relevant academic research and scientific papers

Ruthenium pincer-catalyzed cross-dehydrogenative coupling of primary alcohols with secondary alcohols under neutral conditions

Srimani, Dipankar,Balaraman, Ekambaram,Gnanaprakasam, Boopathy,Ben-David, Yehoshoa,Milstein, David

supporting information, p. 2403 - 2406 (2012/11/07)

Cross-dehydrogenative coupling of primary alcohols with secondary alcohols to obtain mixed esters with the liberation of molecular hydrogen is achieved in high yield and good selectivity under neutral conditions, using a bipyridyl-based PNN ruthenium(II) pincer catalyst. Copyright

A metal-free oxidative esterification of the benzyl C-H bond

Feng, Jie,Liang, Shuai,Chen, Shan-Yong,Zhang, Ji,Fu, Song-Sen,Yu, Xiao-Qi

experimental part, p. 1287 - 1292 (2012/06/15)

An efficient metal-free oxidative esterification of benzyl C-H bonds was developed. Using tetrabutylammonium iodide as catalyst and tert-butyl hydroperoxide as co-oxidant, benzylic substrates could react smoothly with various carboxylic acids to give the esters with good to excellent yields. The method was also suitable for the O-protection of N-Boc amino acids. The reaction mechanism was primarily investigated and a radical process was proposed. Copyright

Ruthenium pincer-catalyzed acylation of alcohols using esters with liberation of hydrogen under neutral conditions

Gnanaprakasam, Boopathy,Ben-David, Yehoshoa,Milstein, David

supporting information; experimental part, p. 3169 - 3173 (2011/02/23)

Acylation of secondary alcohols using non-activated esters, in particular symmetrical esters (such as ethyl acetate), is achieved under neutral conditions with the liberation of molecular hydrogen. This unprecedented, environmentally benign reaction is homogenously catalyzed by a dearomatized ruthenium pincer PNN complex. Copyright

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