17696-64-9 Usage
Description
Butan-2-yl 2-chloroacetate is a chemical compound with the formula C6H11ClO2. It is an ester, formed from the reaction between the carboxylic acid chloroacetic acid and the alcohol butan-2-ol. This colorless liquid possesses a slightly fruity odor and is considered to be moderately toxic, causing irritation to the skin, eyes, and respiratory system.
Uses
Used in Pharmaceutical Industry:
Butan-2-yl 2-chloroacetate is used as a chemical intermediate for the production of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the synthesis of drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, butan-2-yl 2-chloroacetate serves as a chemical intermediate in the development of agrochemicals. Its role in the synthesis process contributes to the creation of products designed to enhance crop protection and yield.
Used as a Solvent:
Butan-2-yl 2-chloroacetate is utilized as a solvent in various industrial applications. Its solvent properties make it suitable for dissolving and mixing with other chemicals in processes such as cleaning, degreasing, and manufacturing.
Used as a Reagent in Organic Synthesis:
butan-2-yl 2-chloroacetate also functions as a reagent in organic synthesis, where it aids in the formation of new chemical bonds and the synthesis of complex organic molecules. Its reactivity and stability make it a valuable tool in the development of new chemical compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 17696-64-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,9 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17696-64:
(7*1)+(6*7)+(5*6)+(4*9)+(3*6)+(2*6)+(1*4)=149
149 % 10 = 9
So 17696-64-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H11ClO2/c1-3-5(2)9-6(8)4-7/h5H,3-4H2,1-2H3
17696-64-9Relevant articles and documents
Synthesis, in silico Study and Antimicrobial Evaluation of New Diesters Derived from Phthaloylglycine
Alves, Francinara S.,Barbosa-Filho, José M.,Cordeiro, Laísa V.,Huang, Min-Fu N.,Lima, Edeltrudes O.,Neto, Hermes Diniz,Souza, Helivaldo D. S.,Trindade, Emmely O.,de Athayde-Filho, Petr?nio F.,de Lima, Priscila S. V.,de Oliveira, Rafael F.,de Sousa, Abra?o P.
, p. 953 - 962 (2020/10/14)
New diesters derived from phthaloylglycine (7a-7i) were synthesized and their structures characterized by infrared, 1H and 13C nuclear magnetic resonance (NMR) spectroscopy. The compounds were evaluated in an in silico study, which demonstrated positive features indicating a possible drug candidate. The diesters showed antifungal activity ranging from moderate to strong against strains of Candida. Compounds 7a, 7b, 7c, 7e and 7i had a moderate minimum inhibitory concentration (MIC) of 1024 μg mL?1 against all fungal strains, while 7h showed a very good MIC of 256 μg mL?1 against Candida albicans, Candida parapsilosis and Candida krusei and 64 μg mL?1 against Candida tropicalis. However, only 7h and 7i were able to inhibit bacterial growth of strains of Staphylococcus aureus, Staphylococcus epidermidis, Pseudomonas aeruginosa and Escherichia coli with an MIC of 1024 μg mL?1
