5038-59-5 Usage
Uses
Used in Organic Synthesis:
4-(2-Bromoacetyl)benzenesulfonyl chloride is used as a synthetic intermediate for the production of various complex chemical compounds. Its unique structure and reactivity make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
In the field of research and development, 4-(2-Bromoacetyl)benzenesulfonyl chloride serves as a key compound for exploring new chemical reactions and developing innovative synthetic pathways. It aids scientists in understanding the properties and behavior of organosulfur compounds and contributes to the advancement of organic chemistry.
Used in Pharmaceutical Industry:
4-(2-Bromoacetyl)benzenesulfonyl chloride is used as a building block in the synthesis of pharmaceutical compounds. Its unique functional groups and reactivity enable the creation of novel drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(2-Bromoacetyl)benzenesulfonyl chloride is employed as a precursor for the development of new pesticides and other crop protection agents. Its versatility in organic synthesis allows for the design of effective and environmentally friendly agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 5038-59-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,3 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5038-59:
(6*5)+(5*0)+(4*3)+(3*8)+(2*5)+(1*9)=85
85 % 10 = 5
So 5038-59-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H6BrClO3S/c9-5-8(11)6-1-3-7(4-2-6)14(10,12)13/h1-4H,5H2
5038-59-5Relevant academic research and scientific papers
Nucleus-independent chemical shift (NICS) as a criterion for the design of new antifungal benzofuranones
González-Chávez, Marco Martín,González-Chávez, Rodolfo,Méndez, Francisco,Martínez, Roberto,Ni?o-Moreno, Perla Del Carmen,Ojeda-Fuentes, Luis Enrique,Richaud, Arlette,Zerme?o-Macías, María de los ángeles
, (2021/08/30)
The assertion made by Wu et al. that aromaticity may have considerable implications for molecular design motivated us to use nucleus-independent chemical shifts (NICS) as an aromaticity criterion to evaluate the antifungal activity of two series of indol-4-ones. A linear regression analysis of NICS and antifungal activity showed that both tested variables were significantly related (p –1 for Candida glabrata, Candida krusei and Candida guilliermondii with compounds 15-32, 15-15 and 15-1. The MIC for filamentous fungi was 1.95 μg·mL–1 for Aspergillus niger for compounds 15-1, 15-33 and 15-34. The results obtained support the use of NICS in the molecular design of compounds with antifungal activity.
Thiazolidine derivatives
-
, (2008/06/13)
The invention relates to thiazolidine derivatives having in 4-position a hydroxy group and a 3'-sulphamyl-phenyl substituent, in 2-position an imino group and in 1-position an aliphatic or cycloaliphatic substituent. Said thiazolidines have diuretic activity. The invention also relates to a process for the manufacture of said compounds.
