10447-11-7 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
4-METHYL-1-NAPHTHALENESULFONYL CHLORIDE is used as a key intermediate for the synthesis of various pharmaceuticals and agrochemicals. Its reactivity and functional group compatibility make it suitable for the development of new drugs and agricultural chemicals.
Used in Dye and Pigment Production:
In the dye and pigment industry, 4-METHYL-1-NAPHTHALENESULFONYL CHLORIDE is utilized as a precursor in the production of dyes and pigments. Its chemical structure contributes to the color properties and stability of the final products.
Used in the Synthesis of Fluorescent Whitening Agents and Optical Brighteners:
4-METHYL-1-NAPHTHALENESULFONYL CHLORIDE is employed as a versatile intermediate in the synthesis of fluorescent whitening agents and optical brighteners. Its unique chemical properties allow for the creation of compounds that enhance the appearance of materials by reflecting light more effectively.
Used in the Production of Resins, Plastics, and Industrial Materials:
4-METHYL-1-NAPHTHALENESULFONYL CHLORIDE is used as a component in the production of resins, plastics, and other industrial materials. Its inclusion in these materials can improve their performance characteristics, such as durability and resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 10447-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10447-11:
(7*1)+(6*0)+(5*4)+(4*4)+(3*7)+(2*1)+(1*1)=67
67 % 10 = 7
So 10447-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H9ClO2S/c1-8-6-7-11(15(12,13)14)10-5-3-2-4-9(8)10/h2-7H,1H3
10447-11-7Relevant academic research and scientific papers
Substituted Disulfonamide Compounds
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Page/Page column 48, (2010/06/22)
Substituted disulfonamide compounds corresponding to formula I: In which R1, R2, R3, R4a, R4b, R5a, R5b, R8, R9a, R9b, R10, R11, a, b, s, t and A have defined meanings, pharmaceutical compositions containing one or more such compounds, processes for preparing such compounds, and a method of using such compounds for the treatment or inhibition of pain and/or other conditions mediated by the bradykinin receptor 1 (BR1).
A practical and efficient preparation of the releasable naphthosultam side chain of a novel anti-MRSA carbapenem
Miller, Ross A.,Humphrey, Guy R.,Lieberman, David R.,Ceglia, Scott S.,Kennedy, Derek J.,Grabowski, Edward J. J.,Reider, Paul J.
, p. 1399 - 1406 (2007/10/03)
A practical large-scale synthesis of the naphthosultam-based side chain of the anti-MRSA antibiotic 1 has been achieved in 29% overall yield over seven steps from 1-methylnaphthalene. The synthesis was completed without the use of protecting groups, featu
