4582-61-0

Basic information

• Product Name: 1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate
• Synonyms: 1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate;6-methylhept-5-en-2-yl 4-methylbenzenesulfonate
• CAS NO: 4582-61-0
• Molecular Formula: C₁₅H₂₂O₃S
• Molecular Weight: 282.39838
• Mol File: 4582-61-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Solubility: Chloroform
• CAS DataBase Reference: 1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate(4582-61-0)
• EPA Substance Registry System: 1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate(4582-61-0)

Safety Data

• Hazardous Substances Data: 4582-61-0(Hazardous Substances Data)

Usage

Description

1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate, also known as 1,5-Dimethyl-4-hexenyl 4-methylbenzenesulfonate, is an organic compound that serves as a protected intermediate in the synthesis of various pharmaceutical compounds. It is characterized by its unique chemical structure, which includes a benzene ring with a sulfonate group and an alkyl chain with multiple methyl groups.

Uses

Used in Pharmaceutical Industry:
1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate is used as a protected intermediate for the synthesis of Isometheptene (I821325), a sympathomimetic amine that exhibits some antihypertensive activity. 1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate plays a crucial role in the development of medications aimed at treating hypertension and other related cardiovascular conditions.
As a protected intermediate, 1,5-DiMethyl-4-hexenyl 4-Methylbenzenesulfonate is essential in the chemical synthesis process, allowing for the formation of the desired active pharmaceutical ingredient (API) with greater efficiency and selectivity. Its use in the pharmaceutical industry highlights its importance in the development of new drugs and therapies for various medical conditions.

Upstream product

• 4630-06-2 6-methylhept-5-en-2-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 110-93-0 6-Methyl-hept-5-en-2-on 

Downstream Products

• 87655-19-4 1-Benzenesulfonyl-4-[2-(1,5-dimethyl-hex-4-enyloxy)-ethoxy]-benzene 
• 344903-14-6 8-Benzenesulfonyl-8-(1,5-dimethyl-hex-4-enyl)-1,4-dioxa-spiro[4.5]dec-6-ene 
• 1723-81-5 zingiberenol 
• 1723-81-5 cis-4-(6-methyl-5-hepten-2-yl)-1-methyl-2-cyclohexen-1-ol 
• 1723-81-5 (1S,4R)-4-(1,5-Dimethyl-hex-4-enyl)-1-methyl-cyclohex-2-enol 
• 100572-83-6 4-(1,5-dimethyl-4-hexenyl)-3-cyclohexen-1-one 
• 1723-81-5 (1R,4R)-1-methyl-4-(6-methylhept-5-en-2-yl)cyclohex-2-enol 
• 1723-80-4 4-(6-methyl-5-hepten-2-yl)-2-cyclohexen-1-one 

Relevant articles and documents

SUBSTITUTED 4H-IMIDAZO [4, 5, 1-IJ] [1, 6] NAPHTHYRIDINE-9-AMINES AND THEIR PHARMACEUTICAL USE

Substituted 4H-imidazo[4,5, 1-ij][1,6]naphthyridine-9-amines of the Formula I : pharmaceutical compositions containing the compounds, intermediates, methods of making the compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.

Sonochemistry of Epoxyalkylhalides in the Presence of a Zinc-Copper Couple

Under sonication in aqueous ethanol, a zinc-copper induces the conjugated addition of epoxyalkyl groups to electron deficient alkenes in synthetically useful yields, provided that the two reducible functionalities are sufficiently far apart; 3,4-epoxyalky