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Benzenesulfonyl chloride, 4-(hexyloxy)-, also known as 4-(hexyloxy)benzenesulfonyl chloride or 4-(Hexyloxy)benzenesulfonyl chloride, is an organic compound with the chemical formula C12H17ClO3S. It is a colorless to pale yellow liquid with a molecular weight of 276.77 g/mol. Benzenesulfonyl chloride, 4-(hexyloxy)- is characterized by the presence of a benzene ring with a sulfonyl chloride group at the para position and a hexyloxy group at the same position. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is typically handled with care and stored under controlled conditions to prevent unwanted reactions.

1145-45-5

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1145-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1145-45-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1145-45:
(6*1)+(5*1)+(4*4)+(3*5)+(2*4)+(1*5)=55
55 % 10 = 5
So 1145-45-5 is a valid CAS Registry Number.

1145-45-5Relevant academic research and scientific papers

CERAMIDE GALACTOSYLTRANSFERASE INHIBITORS FOR THE TREATMENT OF DISEASE

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Paragraph 00204; 00206; 00427; 00428, (2018/07/29)

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with the enzyme ceramide galactosyltransferase (CGT), such as, for example, lysosomal storage diseases. Examples of lysosomal storage diseases include, for example, Krabbe disease and Metachromatic Leukodystrophy.

NOVEL SEMI-SYNTHETIC GLYCOPEPTIDES AS ANTIBACTERIAL AGENTS

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, (2015/03/06)

Semi-synthetic glycopeptides having antibacterial activity are described, in particular, the semi-synthetic glycopeptides described herein are made by chemical modification of the a glycopeptide (Compound A, Compound B, Compound H or Compound C) or the monosaccharide made by hydrolyzing the disaccharide moiety of the amino acid-4 of the parent glycopeptide in acidic medium to give the amino acid-4 monosaccharide; conversion of the monosaccharide to the amino-sugar derivative; acylation of the amino substituent on the amino acid-4 amino-substituted sugar moiety on these scaffolds with certain acyl groups; conversion of the amide group in amino acid-3 on these scaffolds to various acylamide, acylsulfonamide, acylsulfonylurea derivatives; aminomethylation with substituent containing sulfonamide or acylsulfonamide group on amino acid-7 through Mannich reaction; and conversion of the acid moiety on the macrocyclic ring of these scaffolds to certain substituted amides. Also provided are methods for the synthesis of the compounds, pharmaceutical compositions containing the compounds, and methods of use of the compounds for the treatment and/or prophylaxis of diseases, especially bacterial infections.

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