29431-25-2 Usage
Uses
Used in Pharmaceutical Synthesis:
(prop-2-en-1-ylsulfanyl)acetyl chloride is utilized as a key building block in the synthesis of various pharmaceuticals. Its ability to form thioesters and thiol esters, along with other sulfur-containing compounds, makes it a valuable asset in the development of new drugs and medications.
Used in Agrochemical Production:
In the agrochemical industry, (prop-2-en-1-ylsulfanyl)acetyl chloride is employed in the production of a range of products. Its versatility in organic synthesis allows for the creation of compounds that can be used in pesticides, herbicides, and other agricultural applications to enhance crop protection and yield.
Used in Specialty Chemicals:
(prop-2-en-1-ylsulfanyl)acetyl chloride also finds application in the realm of specialty chemicals, where it contributes to the development of unique chemical products that serve specific industries and purposes.
Used in Polymer Production:
(prop-2-en-1-ylsulfanyl)acetyl chloride is used in the production of polymers, thanks to its capacity to form crosslinks within polymer chains. This attribute enhances the strength and durability of the resulting materials, making them suitable for a variety of applications.
Used as a Crosslinking Agent in Material Manufacturing:
In addition to its role in polymer production, (prop-2-en-1-ylsulfanyl)acetyl chloride is also used as a crosslinking agent in the manufacturing of various materials. Its ability to create strong bonds between molecules contributes to the improved performance and stability of the final products.
Check Digit Verification of cas no
The CAS Registry Mumber 29431-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,3 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29431-25:
(7*2)+(6*9)+(5*4)+(4*3)+(3*1)+(2*2)+(1*5)=112
112 % 10 = 2
So 29431-25-2 is a valid CAS Registry Number.
29431-25-2Relevant academic research and scientific papers
Rabasa-Alca?iz, Fernando,Sánchez-Roselló, Mariá,Fustero, Santos,Del Pozo, Carlos
, p. 10785 - 10795 (2019)
The organocatalytic synthesis of indolizinones and pyrrolo-azepinones has been accomplished in a tandem fashion through a sequence that comprises initial cycloaromatization followed by intramolecular Friedel-Crafts alkylation. The process takes place under Br?nsted acid catalysis, giving rise to final products in moderate to good yields. Attempts to carry out the tandem protocol in an enantioselective fashion were performed with chiral (R)-BINOL-derived N-triflyl phosphoramides. After initial optimization, the tandem process took place with moderate levels of enantioselectivity.
7-Amino 2-lower alkyl-2 or 3-cephem-4-carboxylic acid derivatives and processes for preparation thereof
-
, (2008/06/13)
A compound of the formula STR1 wherein R1 is amino or substituted amino, R2 is carboxy or protected carboxy, R3 is lower alkyl and X is --S-- or STR2 or a pharmaceutically acceptable salt thereof is effective against vario
