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Allyl Tiglate, also known as 2-methyl-2-butenoic acid 2-propen-1-yl ester, is a colorless liquid with a strong, fruity odor. It is a naturally occurring compound found in various fruits, such as passion fruit, mango, and pineapple, and is widely used in the flavor and fragrance industry. As a synthetic compound, Allyl Tiglate is produced through the esterification of allyl alcohol and tiglic acid, and it is known for its ability to enhance the aroma of various products, particularly in the creation of tropical and fruity scents. It is also used as a solvent and a chemical intermediate in the synthesis of other compounds. Due to its potential skin and eye irritation, it is important to handle Allyl Tiglate with care and in accordance with safety guidelines.

7493-71-2

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7493-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7493-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7493-71:
(6*7)+(5*4)+(4*9)+(3*3)+(2*7)+(1*1)=122
122 % 10 = 2
So 7493-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O2/c1-4-6-10-8(9)7(3)5-2/h4-5H,1,6H2,2-3H3/b7-5+

7493-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-enyl (E)-2-methylbut-2-enoate

1.2 Other means of identification

Product number -
Other names UNII-VVM5VQM38Z

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:7493-71-2 SDS

7493-71-2Downstream Products

7493-71-2Relevant academic research and scientific papers

Rhenium-catalyzed allylation of C-H bonds of benzoic and acrylic acids

Kuninobu, Yoichiro,Ohta, Kazuhiro,Takai, Kazuhiko

supporting information; experimental part, p. 10791 - 10793 (2011/11/05)

We have succeeded in the allylation of aromatic and olefinic C-H bonds of benzoic and acrylic acids using a rhenium catalyst, Re2(CO) 10. In this reaction, isomerization of the introduced allyl group to the 1-propenyl group did not occur.

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