60548-61-0

Basic information

• Product Name: 1,10-Decanediol, bisulfamate (ester)
• Synonyms: 1,10-Decanediol, bisulfamate (ester)
• CAS NO: 60548-61-0
• Molecular Formula: C10H24 N2 O6 S2
• Molecular Weight: 332.44
• Mol File: 60548-61-0.mol

Chemical Properties

• Boiling Point: 490.3°C at 760 mmHg
• Flash Point: 250.3°C
• Appearance: /
• Density: 1.299g/cm³
• Vapor Pressure: 9.24E-10mmHg at 25°C
• Refractive Index: 1.511
• CAS DataBase Reference: 1,10-Decanediol, bisulfamate (ester)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,10-Decanediol, bisulfamate (ester)(60548-61-0)
• EPA Substance Registry System: 1,10-Decanediol, bisulfamate (ester)(60548-61-0)

Safety Data

• Hazardous Substances Data: 60548-61-0(Hazardous Substances Data)

Usage

Chemical structure

A chemical compound formed from the esterification of 1,10-decanediol with bisulfamic acid.

Applications

Reagent in organic synthesis
Surfactant in emulsion polymerization
Production of plastics, adhesives, and textile chemicals
Personal care products and pharmaceuticals (due to antimicrobial properties)

Industrial uses

Diverse applications due to its unique properties and versatility.

Functional groups

Contains ester and bisulfamate functional groups.

Physical properties

The specific physical properties (e.g., melting point, boiling point, density, etc.) are not provided in the material.

Chemical properties

The specific chemical properties (e.g., reactivity, stability, etc.) are not provided in the material.

Safety and handling

Information on safety precautions, hazard classification, and handling guidelines is not provided in the material.

Environmental impact

The environmental impact of 1,10-Decanediol, bisulfamate (ester) is not discussed in the material.

Synthesis

The synthesis process for 1,10-Decanediol, bisulfamate (ester) is not described in the material.

InChI:InChI=1/C10H24N2O6S2/c11-19(13,14)17-9-7-5-3-1-2-4-6-8-10-18-20(12,15)16/h1-10H2,(H2,11,13,14)(H2,12,15,16)

Upstream product

• 112-47-0 1,10-Decanediol 

Relevant articles and documents

Carbonic anhydrase inhibitors: Synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with bis-sulfamates

A series of bis-sulfamates incorporating aliphatic, aromatic, or betulinyl moieties in their molecules was obtained by reaction of the corresponding diols/diphenols with sulfamoyl chloride. The library of bis-sulfamates thus obtained was tested for the inhibition of three physiologically relevant human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes, the cytosolic hCA I and II, and the transmembrane, tumor-associated hCA IX. The new compounds reported here inhibited hCA I with KI s in the range of 79 nM-16.45 μM, hCA II with KI s in the range of 6-643 nM, and hCA IX with KI s in the range of 4-5400 nM. Several low nanomolar hCA IX inhibitors were detected, such as 1,8-octylene-bis-sulfamate or 1,10-decylene-bis-sulfamate (KI s in the range of 4-7 nM), which showed good selectivity ratios (in the range of 3.50-3.85) for hCA IX over hCA II inhibition. The most selective hCA IX inhibitor was phenyl-1,4-dimethylene-bis-sulfamate (K I of 61.6 nM), which was a 10.43 times better hCA IX than hCA II inhibitor. These derivatives are interesting candidates for the development of novel antitumor therapies targeting hypoxic tumors, since hCA IX is highly overexpressed in such tissues, and its presence is correlated with bad prognosis and unfavorable clinical outcome.

Synthesis and Evaluation of the Male Antifertility Properties of a Series of N-Unsubstituted Sulfamates

A series of six aliphatic and one carbocyclic N-unsubstituted sulfamates have been synthesized and evaluated as potential male antifertility agents.Three of the aliphatic sulfamates 1,2-ethanediyl sulfamate (1), 1,3-propanediyl sulfamate (2), and 1,4-butanediyl sulfamate (3), when administered orally to male rats caused a decrease in the number of pregnant females and/or implantation coupled with increased embryonic and fetal resorption.The compounds were prepared by treating the appropriate glycol salt with sulfamoyl chloride or by the cleavage of a tert-butylsulfamate with trifluoroacetic acid.