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53774-20-2

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53774-20-2 Usage

Description

2-Methyl-3-butenoic acid, also known as alpha-isopropylacrylic acid, is a colorless to light yellow liquid with a fruity odor. It is a carboxylic acid with the chemical formula C5H8O2, known for its versatile applications in various industries due to its unique chemical properties.

Uses

Used in Flavor and Fragrance Industry:
2-Methyl-3-butenoic acid is used as a flavoring agent for imparting fruity notes in various food and beverage products. Its distinctive aroma makes it a valuable ingredient in the creation of artificial fruit flavors.
Used in Polymer Production:
2-Methyl-3-butenoic acid serves as a monomer in the synthesis of polymers, contributing to the development of materials with specific properties tailored for various applications, such as coatings, adhesives, and plastics.
Used in Pharmaceutical Industry:
2-Methyl-3-butenoic acid is used as a pharmaceutical intermediate, playing a crucial role in the synthesis of various drugs. Its chemical structure allows for the development of new medications with potential therapeutic benefits.
Used in Chemical Synthesis:
2-Methyl-3-butenoic acid acts as a precursor in the synthesis of other chemicals, including natural products and pharmaceutical intermediates. Its reactivity and functional groups enable the production of a wide range of compounds with diverse applications.
Safety Considerations:

Check Digit Verification of cas no

The CAS Registry Mumber 53774-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,7 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53774-20:
(7*5)+(6*3)+(5*7)+(4*7)+(3*4)+(2*2)+(1*0)=132
132 % 10 = 2
So 53774-20-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O2/c1-3-4(2)5(6)7/h3-4H,1H2,2H3,(H,6,7)

53774-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylbut-3-enoic acid

1.2 Other means of identification

Product number -
Other names CH2=CHCH(CH3)COOH

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:53774-20-2 SDS

53774-20-2Relevant articles and documents

Nickel-catalyzed electrocarboxylation of allylic halides with CO2

Wu, La-Xia,Deng, Fang-Jie,Wu, Lin,Wang, Huan,Chen, Tai-Jie,Guan, Ye-Bin,Lu, Jia-Xing

, p. 13137 - 13141 (2021/08/03)

Nickel-catalyzed regioselective electrocarboxylation of allylic halides with CO2at atmospheric pressure has been developed by adjusting reaction parameters, including catalyst, solvent, temperature and additive. β,γ-Unsaturated carboxylic acids were obtained in moderate to good yields and with high chain selectivity. This reaction shows tolerance to functional groups. In addition, cyclic voltammetry was performed to provide the possible mechanism of nickel-catalyzed CO2allylation.

By using a palladium amidocarbonyl manufacturing method

-

Page 16, (2008/06/13)

The present invention relates to a process for the preparation of beta- or gamma-unsaturated or saturated carboxylic acids. It relates more particularly to the hydroxycarbonylation of an organic compound comprising a conjugated unsaturation, such as butadiene, by the action of carbon monoxide and water in the presence of a palladium-based catalyst. The carboxylic acids thus obtained are preferably pentenoic acids. According to the invention, the reaction medium after the end of the hydroxycarbonylation stage is treated with hydrogen to reduce the palladium present in the 2+ oxidation state to palladium in the zero oxidation state and the precipitated palladium is recovered.

Conjugate addition of organolithium reagents to α,β-unsaturated carbocyclic acids

Aurell, Maria Jose,Domingo, Luis Ramon,Mestres, Ramon,Munos, Elena,Zaragoza, Ramon Jose

, p. 815 - 830 (2007/10/03)

Conjugate addition of primary, secondary, tertiary alkyi and phenyl lithium reagents to 2-alkenoic acids affords good yields of branched saturated carboxylic acids. Methyl groups at the α- and β-carbon of the 2-alkenoic acid decrease reactivity as acceptors, and foster deprotonation, respectively. The lithium enediolate resulting from the conjugate addition can react with electrophiles. PM3 calculations are in agreement with the substituent effects.

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