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61692-83-9

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61692-83-9 Usage

General Description

Propyl tiglate is a chemical compound with the molecular formula C9H16O2. It is an ester, meaning it is formed from the reaction of a carboxylic acid with an alcohol. Propyl tiglate is commonly found in a variety of fruits, including apples, bananas, and strawberries, where it contributes to their characteristic aroma and flavor. It is also used in the production of perfumes and fragrances due to its fruity and floral scent. In addition, propyl tiglate has been studied for its potential application in pharmaceuticals and as an insect repellant. Overall, propyl tiglate plays an important role in the smell and taste of various fruits and is utilized in a range of industrial and commercial products.

Check Digit Verification of cas no

The CAS Registry Mumber 61692-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,9 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61692-83:
(7*6)+(6*1)+(5*6)+(4*9)+(3*2)+(2*8)+(1*3)=139
139 % 10 = 9
So 61692-83-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c1-4-6-10-8(9)7(3)5-2/h5H,4,6H2,1-3H3/b7-5+

61692-83-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name propyl (E)-2-methylbut-2-enoate

1.2 Other means of identification

Product number -
Other names EINECS 262-906-4

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:61692-83-9 SDS

61692-83-9Downstream Products

61692-83-9Relevant articles and documents

Stereo- and chemoselective cross-coupling between two electron-deficient acrylates: An efficient route to (Z, E)-muconate derivatives

Hu, Xu-Hong,Zhang, Jian,Yang, Xiao-Fei,Xu, Yun-He,Loh, Teck-Peng

supporting information, p. 3169 - 3172 (2015/03/30)

A Ru-catalyzed direct oxidative cross-coupling reaction of acrylates was developed. It offers a straightforward and atom-economical protocol for the synthesis of functionalized (Z,E)-muconate derivatives in moderate to good yields with good stereo- and chemoselectivities. The conjugated muconates bearing differentiable terminal functionality can be selectively transformed into versatile synthetic intermediates widely used in organic synthesis.

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