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Propyl tiglate, with the molecular formula C9H16O2, is an ester derived from the reaction of a carboxylic acid with an alcohol. It is naturally present in a variety of fruits such as apples, bananas, and strawberries, where it imparts their distinctive aroma and flavor. Known for its fruity and floral scent, propyl tiglate is also utilized in the production of perfumes and fragrances. Moreover, it has been investigated for its potential pharmaceutical applications and as an insect repellent, highlighting its multifaceted role in both the natural world and various industrial sectors.

61692-83-9

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61692-83-9 Usage

Uses

Used in Flavor and Fragrance Industry:
Propyl tiglate is used as a flavoring agent for its characteristic fruity and floral notes, enhancing the taste and aroma of various fruits, particularly apples, bananas, and strawberries.
Used in Perfumery:
Propyl tiglate is used as a fragrance ingredient for its pleasant and appealing scent, contributing to the creation of perfumes and other scented products.
Used in Pharmaceutical Industry:
Propyl tiglate is studied for its potential application in pharmaceuticals, indicating its possible use as an active ingredient or component in medicinal formulations.
Used in Insect Repellent Industry:
Propyl tiglate has been researched for its potential as an insect repellent, suggesting its use in developing products to deter insects and protect against bites.

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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