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2-Phenylethyl dodecanoate, also known as 2-phenylethyl laurate, is an organic compound with the chemical formula C18H26O2. It is a colorless to pale yellow liquid with a fruity, floral, and slightly sweet odor. This ester is formed by the reaction of 2-phenylethanol and dodecanoic acid, and it is commonly used in the fragrance and flavor industries due to its pleasant scent, which resembles a combination of rose and jasmine. It can be found in various natural sources, such as flowers and fruits, and is also used as a fixative in perfumes to help stabilize and prolong the fragrance. Additionally, 2-phenylethyl dodecanoate has potential applications in the pharmaceutical and cosmetic industries.

6309-54-2

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6309-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6309-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6309-54:
(6*6)+(5*3)+(4*0)+(3*9)+(2*5)+(1*4)=92
92 % 10 = 2
So 6309-54-2 is a valid CAS Registry Number.

6309-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylethyl dodecanoate

1.2 Other means of identification

Product number -
Other names phenethyl dodecanoate

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:6309-54-2 SDS

6309-54-2Downstream Products

6309-54-2Relevant academic research and scientific papers

A novel aromatic carbocation-based coupling reagent for esterification and amidation reactions

Nguyen, Thanh V.,Lyons, Demelza J.M.

supporting information, p. 3131 - 3134 (2015/06/17)

A novel tropylium-based coupling reagent has been developed to facilitate the synthesis of a series of esters, amides, lactones and peptides under mild reaction conditions. Remarkably, this reagent can be used in catalytic amounts in conjunction with a sacrificial reagent, offering a new and efficient method for nucleophilic coupling reactions of carboxylic acids.

Heterobimetallic dinuclear lanthanide alkoxide complexes as acid-base difunctional catalysts for transesterification

Zeng, Ruijie,Sheng, Hongting,Zhang, Yongcang,Feng, Yan,Chen, Zhi,Wang, Junfeng,Chen, Man,Zhu, Manzhou,Guo, Qingxiang

, p. 9246 - 9252 (2014/12/11)

A practical lanthanide(III)-catalyzed transesterification of carboxylic esters, weakly reactive carbonates, and much less-reactive ethyl silicate with primary and secondary alcohols was developed. Heterobimetallic dinuclear lanthanide alkoxide complexes [Ln2Na8{(OCH2CH2NMe2)}12(OH)2] (Ln = Nd (I), Sm (II), and Yb (III)) were used as highly active catalysts for this reaction. The mild reaction conditions enabled the transesterification of various substrates to proceed in good to high yield. Efficient activation of transesterification may be endowed by the above complexes as cooperative acid-base difunctional catalysts, which is proposed to be responsible for the higher reactivity in comparison with simple acid/base catalysts.

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