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Home Sulfos Methanesulfonothioic acid, S-ethyl ester

Methanesulfonothioic acid, S-ethyl ester

CAS No.:
2043-76-7
Catalog Number:
AG0029ER
Molecular Formula:
C3H8O2S2
Molecular Weight:
140.2244
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Product Description
Catalog Number:
AG0029ER
Chemical Name:
Methanesulfonothioic acid, S-ethyl ester
CAS Number:
2043-76-7
Molecular Formula:
C3H8O2S2
Molecular Weight:
140.2244
MDL Number:
MFCD09842607
IUPAC Name:
1-methylsulfonylsulfanylethane
InChI:
InChI=1S/C3H8O2S2/c1-3-6-7(2,4)5/h3H2,1-2H3
InChI Key:
IZAYCFBWPSFFJI-UHFFFAOYSA-N
SMILES:
CCSS(=O)(=O)C
Properties
Complexity:
118  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
139.997g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
140.215g/mol
Monoisotopic Mass:
139.997g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
67.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.4  
Literature
Title Journal
A gadolinium triacetic monoamide DOTA derivative with a methanethiosulfonate anchor group. Relaxivity properties and conjugation with albumin and thiolated particles. Contrast media & molecular imaging 20070101
Open probability of the epithelial sodium channel is regulated by intracellular sodium. The Journal of physiology 20060715
Substituted cysteine accessibility of the third transmembrane domain of the creatine transporter: defining a transport pathway. The Journal of biological chemistry 20050923
Role of charged residues in coupling ligand binding and channel activation in the extracellular domain of the glycine receptor. The Journal of biological chemistry 20031212
Thiol-reactive luminescent lanthanide chelates: part 2. Bioconjugate chemistry 20030101
Properties