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61692-84-0

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61692-84-0 Usage

General Description

Isobutyl tiglate is an organic chemical compound belonging to the ester class, characterized by a fruity and floral odor. It is commonly used as a flavoring agent in the food and beverage industry, as well as in the formulation of perfumes and cosmetics. Isobutyl tiglate is also known for its insecticidal properties, making it a potentially effective ingredient in pest control products. Its chemical structure consists of a tiglic acid moiety and an isobutyl group, which contribute to its distinctive scent and functional properties. Overall, isobutyl tiglate is a versatile compound with applications in fragrance, flavor, and pest control industries.

Check Digit Verification of cas no

The CAS Registry Mumber 61692-84-0 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 61692-84:
(7*6)+(6*1)+(5*6)+(4*9)+(3*2)+(2*8)+(1*4)=140
140 % 10 = 0
So 61692-84-0 is a valid CAS Registry Number.

61692-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Isobutyl Tiglate

1.2 Other means of identification

Product number -
Other names ISOBUTYL TIGLATE

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:61692-84-0 SDS

61692-84-0Downstream Products

61692-84-0Relevant articles and documents

Asymmetric dihydroxylation of esters and amides of methacrylic, tiglic, and angelic acid: No exception to the sharpless mnemonic!

Weber, Fabian,Brückner, Reinhard

, p. 2428 - 2449 (2015/04/22)

Literature findings on the facial selectivity of the Sharpless asymmetric dihydroxylation (SAD) of isobutyl angelate are contradictory and partly in conflict with the Sharpless mnemonic. We systematically screened the SAD of esters and amides of angelic, tiglic, and methacrylic acid. Enantiocontrol arose in 14 of the 15 reactions, culminating at 99 % ee for the Weinreb amide of tiglic acid. The absolute configurations of all the nonracemic products were established by (stereo)chemical correlations. Without exception, they conform to the Sharpless mnemonic.

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