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2-Butenoic acid, 3-(3,4-dimethoxyphenyl)-, ethyl ester is a chemical compound with the molecular formula C13H16O4. It is an ester derivative of 2-butenoic acid, featuring a 3,4-dimethoxyphenyl group attached to the third carbon of the butenoic acid chain. 2-Butenoic acid, 3-(3,4-dimethoxyphenyl)-, ethyl ester is characterized by its fruity and floral aroma, making it a valuable component in the fragrance industry. It is used in the creation of perfumes and other scented products due to its pleasant odor. The ethyl ester group in its structure contributes to its volatility and ability to release the scent when applied. It is important to note that, like many chemicals, it should be handled with care due to potential irritancy or other health effects, and its use is subject to safety regulations and guidelines.

7706-60-7

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7706-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7706-60-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7706-60:
(6*7)+(5*7)+(4*0)+(3*6)+(2*6)+(1*0)=107
107 % 10 = 7
So 7706-60-7 is a valid CAS Registry Number.

7706-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3,4-dimethoxy-phenyl)-crotonic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 3-(3,4-Dimethoxy-phenyl)-crotonsaeure-aethylester

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:7706-60-7 SDS

7706-60-7Relevant academic research and scientific papers

Simple, copper(I)-catalyzed oxidation of benzylic/allylic alcohols to carbonyl compounds: Synthesis of functionalized cinnamates in one pot

Reddy, Alavala Gopi Krishna,Mahendar, Lodi,Satyanarayana, Gedu

, p. 2076 - 2087 (2014/07/07)

An environmentally benign [Cu(I)]-catalyzed oxidation of activated (benzylic/allylic) alcohols to the corresponding carbonyl compounds is presented. Interestingly, the reaction was also compatible with benzylic alcohols containing ortho-bromo substituents on the aromatic ring without competing with the expected intermolecular Buchwald coupling. Significantly, the catalytic system enables the synthesis of cinnamate-esters in a sequential domino one-pot fashion via oxidation followed by Wittig-Horner protocol. Copyright

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