Home Other Building Blocks Formamide, N,N-diethyl-1-(methylsulfinyl)-

Formamide, N,N-diethyl-1-(methylsulfinyl)-

CAS No.:
140703-15-7
Catalog Number:
AG001CPV
Molecular Formula:
C6H13NO2S
Molecular Weight:
163.2379
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Product Description
Catalog Number:
AG001CPV
Chemical Name:
Formamide, N,N-diethyl-1-(methylsulfinyl)-
CAS Number:
140703-15-7
Molecular Formula:
C6H13NO2S
Molecular Weight:
163.2379
MDL Number:
MFCD00870745
IUPAC Name:
N,N-diethyl-1-methylsulfinylformamide
InChI:
InChI=1S/C6H13NO2S/c1-4-7(5-2)6(8)10(3)9/h4-5H2,1-3H3
InChI Key:
FQSRGOGWCPXJIN-UHFFFAOYSA-N
SMILES:
CCN(C(=O)S(=O)C)CC
Properties
Complexity:
143  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
163.067g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
163.235g/mol
Monoisotopic Mass:
163.067g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
56.6A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
0
Literature
Title Journal
Antitubercular activity of disulfiram, an antialcoholism drug, against multidrug- and extensively drug-resistant Mycobacterium tuberculosis isolates. Antimicrobial agents and chemotherapy 20120801
Persistent pain is dependent on spinal mitochondrial antioxidant levels. The Journal of neuroscience : the official journal of the Society for Neuroscience 20090107
Disulfiram metabolites permanently inactivate the human multidrug resistance P-glycoprotein. Molecular pharmaceutics 20040101
Chemical modifications to study mutations that affect the ability of the general base (E268) to function in human liver mitochondrial aldehyde dehydrogenase. Chemico-biological interactions 20030201
Metabolism of a disulfiram metabolite, S-methyl N,N-diethyldithiocarbamate, by flavin monooxygenase in human renal microsomes. Drug metabolism and disposition: the biological fate of chemicals 20010201
Overview--in vitro inhibition of aldehyde dehydrogenase by disulfiram and metabolites. Chemico-biological interactions 20010130
In vivo inhibition of aldehyde dehydrogenase by disulfiram. Chemico-biological interactions 20010130
S-methyl-N,N-diethylthiocarbamate sulfoxide elicits neuroprotective effect against N-methyl-D-aspartate receptor-mediated neurotoxicity. Journal of biomedical science 20010101
Rat liver constitutive and phenobarbital-inducible cytosolic aldehyde dehydrogenases are highly homologous proteins that function as distinct isozymes. Biochemistry 20000912
Properties