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Ethyl 2-butyl-2-phenylhexanoate is a complex organic compound with the chemical formula C20H32O2. It is an ester derived from the combination of 2-butyl-2-phenylhexanoic acid and ethanol. This colorless to pale yellow liquid is characterized by a fruity, floral, and slightly woody odor, making it a valuable component in the fragrance industry. It is used in the creation of perfumes and other scented products due to its ability to provide a rich, long-lasting aroma. The compound is also known for its low toxicity and is considered safe for use in cosmetics and personal care products when used within recommended concentrations.

2901-15-7

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2901-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2901-15-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2901-15:
(6*2)+(5*9)+(4*0)+(3*1)+(2*1)+(1*5)=67
67 % 10 = 7
So 2901-15-7 is a valid CAS Registry Number.

2901-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-butyl-2-phenylhexanoate

1.2 Other means of identification

Product number -
Other names 2-butyl-2-phenyl-hexanoic acid ethyl 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:2901-15-7 SDS

2901-15-7Relevant academic research and scientific papers

Pd(II)-catalyzed enantioselective C-H activation/C-O bond formation: Synthesis of chiral benzofuranones

Cheng, Xiu-Fen,Li, Yan,Su, Yi-Ming,Yin, Feng,Wang, Jian-Yong,Sheng, Jie,Vora, Harit U.,Wang, Xi-Sheng,Yu, Jin-Quan

supporting information, p. 1236 - 1239 (2013/03/14)

Pd(II)-catalyzed enantioselective C-H activation of phenylacetic acids followed by an intramolecular C-O bond formation afforded chiral benzofuranones. This reaction provides the first example of enantioselecctive C-H functionalizations through Pd(II)/Pd(IV) redox catalysis.

HIGHLY DISPERSED POTASSIUM ON ALUMINA AS A METALATING AGENT. ALKYLATION OF ENOLIZABLE COMPOUNDS

Savoia, Diego,Tagliavini, Emilio,Trombini, Claudio,Umani-Ronchi, Achille

, p. 281 - 286 (2007/10/02)

Highly dispersed potassium on alumina (K/Al2O3) acts as a metalating agent towards enolizable compounds and the intermediate organopotassium derivatives can be alkylated with primary alkyl bromides.The reaction conditions are dependent on the substrate.In particular, tetrahydrofuran is the solvent of choice for the metalation of nitriles and aldehyde N,N-dimethylhydrazones at -60 deg C and of N-cyclohexyl ketimines at room temperature, whereas hexane must be used for ketones.

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