CAS 196929-78-9 | (R)-(+)-2-Methyl-2-Propanesulfinamide | CAS Number 196929-78-9

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196929-78-9 | (R)-(+)-2-Methyl-2-Propanesulfinamide

CAS No: 196929-78-9 Catalog No: AG0032E1 MDL No:MFCD01863616

Product Description

Catalog Number:

AG0032E1

Chemical Name:

(R)-(+)-2-Methyl-2-Propanesulfinamide

CAS Number:

196929-78-9

Molecular Formula:

C4H11NOS

Molecular Weight:

121.2012

MDL Number:

MFCD01863616

IUPAC Name:

(R)-2-methylpropane-2-sulfinamide

InChI:

InChI=1S/C4H11NOS/c1-4(2,3)7(5)6/h5H2,1-3H3/t7-/m1/s1

InChI Key:

CESUXLKAADQNTB-SSDOTTSWSA-N

SMILES:

CC([S@@](=O)N)(C)C

EC Number:

676-338-3

Properties

Complexity:

84.2

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

121.056g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

121.198g/mol

Monoisotopic Mass:

121.056g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

62.3A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

Literature

Title	Journal
(R)-N-(3-Meth-oxy-phen-yl)-tert-butane-sulfinamide.	Acta crystallographica. Section E, Structure reports online 20120301
A novel asymmetric synthesis of cinacalcet hydrochloride.	Beilstein journal of organic chemistry 20120101
Stereoselective synthesis of novel uracil polyoxin C conjugates as substrate analogues of chitin synthase.	The Journal of organic chemistry 20080516
Synthesis of enantiopure tert-butanesulfinamide from tert-butanesulfinyloxazolidinone.	The Journal of organic chemistry 20041126
Properly designed modular asymmetric synthesis for enantiopure sulfinamide auxiliaries from N-sulfonyl-1,2,3-oxathiazolidine-2-oxide agents.	Journal of the American Chemical Society 20020710