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144-76-3 | Methanesulfinic acid, 1,1'-[sulfonylbis(4,1-phenyleneimino)]bis-
CAS No: 144-76-3 Catalog No: AG001IR0 MDL No:
Product Description
Catalog Number:
AG001IR0
Chemical Name:
Methanesulfinic acid, 1,1'-[sulfonylbis(4,1-phenyleneimino)]bis-
CAS Number:
144-76-3
Molecular Formula:
C14H16N2O6S3
Molecular Weight:
404.4816
IUPAC Name:
[4-[4-(sulfinomethylamino)phenyl]sulfonylanilino]methanesulfinic acid
InChI:
InChI=1S/C14H16N2O6S3/c17-23(18)9-15-11-1-5-13(6-2-11)25(21,22)14-7-3-12(4-8-14)16-10-24(19)20/h1-8,15-16H,9-10H2,(H,17,18)(H,19,20)
InChI Key:
NEDPPCHNEOMTJV-UHFFFAOYSA-N
SMILES:
OS(=O)CNc1ccc(cc1)S(=O)(=O)c1ccc(cc1)NCS(=O)O
UNII:
0G3C18OH4D
Properties
Complexity:
520
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
404.017g/mol
Formal Charge:
0
Heavy Atom Count:
25
Hydrogen Bond Acceptor Count:
10
Hydrogen Bond Donor Count:
4
Isotope Atom Count:
0
Molecular Weight:
404.47g/mol
Monoisotopic Mass:
404.017g/mol
Rotatable Bond Count:
8
Topological Polar Surface Area:
180A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.2
Literature
| Title | Journal |
|---|---|
| Remission in dermatitis herpetiformis: a cohort study. | Archives of dermatology 20110301 |
| Impact of glycemic control on the incidence of acute kidney injury in critically ill patients: a comparison of two strategies using the RIFLE criteria. | Clinics (Sao Paulo, Brazil) 20100801 |
| Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors. | Journal of medicinal chemistry 20081113 |
| Beneficial effects of a diabetes specific formula on insulin sensitivity and free fatty acid in patients with type 2 diabetes mellitus. | Chinese medical journal 20080420 |
| Total synthesis of azumamide A and azumamide E, evaluation as histone deacetylase inhibitors, and design of a more potent analogue. | Organic letters 20070315 |
| Diastereomerically and enantiomerically pure 2,3-disubstituted pyrrolidines from 2,3-aziridin-1-ols using a sulfoxonium ylide: a one-carbon homologative relay ring expansion. | Journal of the American Chemical Society 20070221 |
| Synthesis of novel test compounds for antiviral chemotherapy of severe acute respiratory syndrome (SARS). | Current medicinal chemistry 20050101 |
| Avoid, attack or do both? Behavioral and physiological adaptations in natural enemies faced with novel hosts. | BMC evolutionary biology 20050101 |
| Asymmetric synthesis of unsaturated, fused bicyclic proline analogues through amino alkylation of cyclic bis(allylsulfoximine)titanium complexes and migratory cyclization of delta-amino alkenyl aminosulfoxonium salts. | Journal of the American Chemical Society 20031029 |
| Asymmetric synthesis of anti-homopropargylic alcohols from aldehydes and chiral sulfonimidoyl substituted bis(allyl)titanium complexes through generation and elimination of novel chiral alkylidenecarbene (dimethylamino)sulfoxonium ylides. | Journal of the American Chemical Society 20020904 |
| p-Sulfooxyphenylpyruvic acid from the red macro alga Ceratodictyon spongiosum and its sponge symbiont Haliclona cymaeformis. | Phytochemistry 20020601 |
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