68631-04-9 Usage
Uses
Used in Pharmaceutical and Agrochemical Production:
2,3-dimethyl-5-nitrobenzene-1-sulphonyl chloride is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides. Its role in these industries is pivotal for creating effective and safe products.
Used in Dye and Pigment Synthesis:
In the dye and pigment industry, 2,3-dimethyl-5-nitrobenzene-1-sulphonyl chloride is utilized as a reagent, playing a crucial part in the creation of a diverse range of colorants used in textiles, paints, and other applications.
Used in Laboratory Research as a Sulfonylating Agent:
2,3-dimethyl-5-nitrobenzene-1-sulphonyl chloride is employed in laboratory settings as a sulfonylating agent, where it is used to introduce sulfonyl groups into organic compounds. This function is essential for advancing chemical research and the development of novel organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 68631-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,6,3 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 68631-04:
(7*6)+(6*8)+(5*6)+(4*3)+(3*1)+(2*0)+(1*4)=139
139 % 10 = 9
So 68631-04-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNO4S/c1-5-3-7(10(11)12)4-8(6(5)2)15(9,13)14/h3-4H,1-2H3
68631-04-9Relevant academic research and scientific papers
Novel sulfamoyl benzamides as selective CB2 agonists with improved in vitro metabolic stability
Sellitto, Ian,Bourdonnec, Bertrand Le,Worm, Karin,Goodman, Allan,Savolainen, Markku A.,Chu, Guo-Hua,Ajello, Christopher W.,Saeui, Christopher T.,Leister, Lara K.,Cassel, Joel A.,DeHaven, Robert N.,LaBuda, Christopher J.,Koblish, Michael,Little, Patrick J.,Brogdon, Bernice L.,Smith, Steven A.,Dolle, Roland E.
scheme or table, p. 387 - 391 (2010/04/06)
A lead optimization campaign in our previously reported sulfamoyl benzamide class of CB2 agonists was conducted to improve the in vitro metabolic stability profile in this series while retaining high potency and selectivity for the CB2 receptor. From this study, compound 14, N-(3,4-dimethyl-5-(morpholinosulfonyl)phenyl)-2,2-dimethylbutanamide, was identified as a potent and selective CB2 agonist exhibiting moderate in vitro metabolic stability and oral bioavailability. Compound 14 demonstrated in vivo efficacy in a rat model of post-surgical pain.
