39720-27-9 Usage
Description
4-(Chloromethyl)phenyl acetate is an organic compound with the chemical formula C9H9ClO2. It is a colorless to pale yellow liquid with a mild, fruity odor. 4-(CHLOROMETHYL)PHENYL ACETATE is characterized by its chloromethyl group attached to a phenyl ring, which provides it with unique reactivity and properties. It is commonly used as a reagent in various chemical reactions and assays due to its versatility and stability.
Uses
Used in Chemical Synthesis:
4-(Chloromethyl)phenyl acetate is used as a reagent in chemical synthesis for the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its chloromethyl group can be easily substituted with other functional groups, making it a valuable building block for the creation of complex molecules.
Used in 4-(Chloromethyl)phenyl Acetate Assay:
4-(Chloromethyl)phenyl acetate is used as a reagent in the 4-(chloromethyl)phenyl acetate assay, which is a method for determining the presence and concentration of this compound in a sample. This assay is essential for quality control and monitoring the purity of the compound in various applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(Chloromethyl)phenyl acetate is used as an intermediate in the synthesis of various drugs. Its unique reactivity allows for the creation of new drug candidates with potential therapeutic benefits.
Used in Agrochemical Industry:
4-(Chloromethyl)phenyl acetate is also used in the agrochemical industry for the synthesis of pesticides and other crop protection agents. Its versatility in chemical reactions enables the development of new compounds with improved efficacy and selectivity.
Used in Research and Development:
In the field of research and development, 4-(Chloromethyl)phenyl acetate is employed as a reagent for studying various chemical reactions and mechanisms. Its unique properties make it an interesting subject for scientific investigation, potentially leading to new discoveries and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 39720-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,2 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39720-27:
(7*3)+(6*9)+(5*7)+(4*2)+(3*0)+(2*2)+(1*7)=129
129 % 10 = 9
So 39720-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClO2/c1-7(11)12-9-4-2-8(6-10)3-5-9/h2-5H,6H2,1H3
39720-27-9Relevant articles and documents
Fluorescent labeling of s2T-incorporated DNA and m5s2U-modified RNA
Yu, Ping,Zhou, Honglin,Li, Yuanyuan,Du, Zhifeng,Wang, Rui
, p. 754 - 766 (2021/07/06)
We report herein comprehensive investigations of alkylation/sulfur exchange reactions of sulfur-containing substrates including nucleosides such as s2U, m5s2U, s4U, s2A and s2T-incorporated DNA enable by comprehensive screenings of the reagents (2a–2h). It has been proven that iodoacetamide (2a) displays the most promising feasibility toward sulfur-containing substrates including s2T, s2U, m5s2U, s4U and s2A. In sharp contrast, the alkylation process with S-benzyl methanethiosulfonate (BMTS, 2h) displays the best application potential only for s4U. Based on these results, the fluorescent labeling of s2T-incorporated DNA and m5s2U-modified RNA has been achieved. Supplemental data for this article is available online at https://doi.org/10.1080/15257770.2021.1942044.
Palladium-catalyzed carboxylative coupling of benzyl chlorides with allyltributylstannane: Remarkable effect of palladium nanoparticles
Feng, Xiujuan,Sun, Anle,Zhang, Sheng,Yu, Xiaoqiang,Bao, Ming
, p. 108 - 111 (2013/04/10)
Palladium-catalyzed carboxylative coupling of benzyl chlorides with allyltributylstannane was successfully conducted to produce benzyl but-3-enoates in satisfactory to good yields. The carboxylative coupling reaction occurred smoothly under mild conditions in the presence of palladium nanoparticles in tetrahydrofuran.
A highly chemoselective and rapid chlorination of benzyl alcohols under neutral conditions
Sun, Lili,Peng, Guisheng,Niu, Hongmei,Wang, Qiang,Li, Chunbao
experimental part, p. 3919 - 3924 (2009/05/26)
A rapid and highly selective chlorination method has been developed using 2,4,6-trichloro-1,3,5-triazine (TCT) catalyzed by dimethyl sulfoxide. The reactions take 10 to 40 minutes, and the yields are almost quantitative. The neutral reaction conditions are compatible with substrates bearing acid-labile functional groups. Both competitive intramolecular and intermolecular reactions for benzyl alcohols in the presence of aliphatic alcohols indicate high selectivity. The procedure has been successfully used in the selective chlorination of gastrodin, a clinically used neuromedicine. This procedure represents a useful new tool in organic and medicinal chemistry. Georg Thieme Verlag Stuttgart.