60586-80-3

Basic information

• Product Name: heptane-1-sulphonic acid
• Synonyms: heptane-1-sulphonic acid;Heptane-1-sulfonic acid;Einecs 262-314-6
• CAS NO: 60586-80-3
• Molecular Formula: C₇H₁₆O₃S
• Molecular Weight: 180.26514
• EINECS: 262-314-6
• Mol File: 60586-80-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Density: 1.108g/cm³
• Refractive Index: 1.463
• CAS DataBase Reference: heptane-1-sulphonic acid(CAS DataBase Reference)
• NIST Chemistry Reference: heptane-1-sulphonic acid(60586-80-3)
• EPA Substance Registry System: heptane-1-sulphonic acid(60586-80-3)

Safety Data

• Hazardous Substances Data: 60586-80-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H16O3S/c1-2-3-4-5-6-7-11(8,9)10/h2-7H2,1H3,(H,8,9,10)

Upstream product

• 142-82-5 n-heptane 
• 5416-94-4 heptylsulfanyl cyanate 
• 25355-20-8 di-n-heptyl sulfoxide 
• 16156-50-6 n-hexyl methanesulfonate 
• 1639-09-4 heptanethiol 
• 7697-37-2 nitric acid 
• 629-04-9 1-Bromoheptane 

Downstream Products

• 927-92-4 heptanesulfonyl chloride 

Relevant articles and documents

Semiconductor-photocatalyzed sulfoxidation of alkanes

(Equation Presented) The C-H activation of alkanes with visible light is possible with a semiconductor as the photocatalyst. Upon irradiation, a mixture of titanium dioxide, sulfur dioxide, and oxygen can be used to convert alkanes into the corresponding sulfonic acids (see scheme).

Foldamers as reactive sieves: Reactivity as a probe of conformational flexibility

A series of m-phenyleneethynylene (mPE) oligomers modified with a dimethylaminopyridine (DMAP) unit were treated with methyl sulfonates of varying sizes and shapes, and the relative reactivities were measured by UV spectrophotometry. Using a small-molecule DMAP analogue as a reference, each of the methyl sulfonates was shown to react at nearly identical rate. In great contrast, oligomers that are long enough to fold, and hence capable of binding the methyl sulfonate, experience rate enhancements of 18-1600-fold relative to that of the small-molecule analogue, depending on the type of alkyl chain attached to the guest. Three different oligomer lengths were studied, with the longest oligomers exhibiting the fastest rate and greatest substrate specificity. Even large, bulky guests show slightly enhanced methylation rates compared to that with the reference DMAP, which suggests a dynamic nature to the oligomer's binding cavity. Several mechanistic models to describe this behavior are discussed.

7-Oxabicycloheptane substituted prostaglandin interphenylene analogs useful in the treatment of thrombolytic disease

7-Oxabicycloheptane substituted interphenylene prostaglandin ethers are provided having the structural formula STR1 and including all stereoisomers thereof. The compounds are cardiovascular agents useful, for example, in the treatment of thrombolytic disease.