22577-15-7 Usage
Description
3-Allyloxypropionic Acid, also known as allyl glycolic acid, is an organic compound with the chemical formula C6H10O3. It is a colorless liquid with a slightly pungent odor and is soluble in water. 3-ALLYLOXYPROPIONIC ACID is characterized by its allyl and carboxyl functional groups, which provide it with unique chemical properties and reactivity.
Uses
Used in Chemical Industry:
3-Allyloxypropionic Acid is used as an intermediate for the synthesis of various chemicals, including plasticizers, which are additives that increase the plasticity or flexibility of materials, particularly in the plastics industry. Its allyl group allows for further chemical modifications and reactions, making it a versatile building block for the development of new compounds and materials.
Used in Plasticizers Production:
3-Allyloxypropionic Acid is used as a key component in the production of plasticizers, which are widely utilized in the manufacturing of polymers and plastics to enhance their workability, flexibility, and durability. The allyl group in 3-allyloxypropionic acid can be further reacted to produce plasticizers with specific properties tailored to various applications, such as in the automotive, construction, and packaging industries.
Check Digit Verification of cas no
The CAS Registry Mumber 22577-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,7 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22577-15:
(7*2)+(6*2)+(5*5)+(4*7)+(3*7)+(2*1)+(1*5)=107
107 % 10 = 7
So 22577-15-7 is a valid CAS Registry Number.
22577-15-7Relevant articles and documents
Preparation of 3-(n-alkenoxy)propanoic acids
Simonot,Rousseau
, p. 549 - 560 (1993)
3-(n-Alkenoxy)propanoic acids have been prepared by reaction of alkenols with tert-butyl acrylate (catalyzed by Triton B or n-butyl lithium) followed by cleavage of the tert-butyl group by CF3COOH or KO2.
Oxidative cyclization of alkenoic acids promoted by AgOAc
Carrillo-Arcos, Ulises A.,Rojas-Ocampo, Jonathan,Porcel, Susana
supporting information, p. 479 - 483 (2016/01/09)
Alkenoic acids derived from salicylic acid and analogues undergo an unexpected oxidative cyclization process triggered by AgOAc leading to 4H-benzo[d][1,3]dioxin-4-ones. The process is affected by the substitution on the aryl and the allyl units.
Kinetics of the Coupling Reactions of the Nitroxyl Radical 1,1,3,3-Tetramethylisoindoline-2-oxyl with Carbon-Centered Radicals
Beckwith, Athelstan L. J.,Bowry, Vincent W.,Moad, Graeme
, p. 1632 - 1641 (2007/10/02)
Radical clocks have been used to study the kinetics of the coupling of the nitroxyl radical 1,1,3,3-tetramethylisoindoline-2-oxyl (T) in cyclohexane or benzene with a variety of carbon-centered radicals including simple unhindered primary, secondary, and
