Home Other Building Blocks N-tert-Butylbenzenesulfinimidoyl chloride

N-tert-Butylbenzenesulfinimidoyl chloride

CAS No.:
49591-20-0
Catalog Number:
AG003TD9
Molecular Formula:
C10H14ClNS
Molecular Weight:
215.7429
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
80%
In Stock USA
United States
$238
- +
5g
80%
In Stock USA
United States
$725
- +
Product Description
Catalog Number:
AG003TD9
Chemical Name:
N-tert-Butylbenzenesulfinimidoyl chloride
CAS Number:
49591-20-0
Molecular Formula:
C10H14ClNS
Molecular Weight:
215.7429
MDL Number:
MFCD03093621
IUPAC Name:
tert-butylimino-chloro-phenyl-λ4-sulfane
InChI:
InChI=1S/C10H14ClNS/c1-10(2,3)12-13(11)9-7-5-4-6-8-9/h4-8H,1-3H3
InChI Key:
RZJYQVFWNHEPTH-UHFFFAOYSA-N
SMILES:
CC(N=S(c1ccccc1)Cl)(C)C
Properties
Complexity:
190  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
215.054g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
215.739g/mol
Monoisotopic Mass:
215.054g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
31.6A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
4.8  
Literature
Title Journal
Direct and efficient one-pot preparation of ketones from aldehydes using N-tert-butylphenylsulfinimidoyl chloride. Organic letters 20061026
Oxidative Mannich reaction of N-carbobenzyloxy amines with 1,3-dicarbonyl compounds. Organic letters 20060914
Imino sulfinamidines: synthesis and coordination chemistry of a novel class of chiral bidentate ligands. Inorganic chemistry 20060417
Highly efficient methods for the one-pot synthesis of beta-substituted enones. Organic & biomolecular chemistry 20060107
One-pot beta-substitution of enones with alkyl groups to beta-alkyl enones. Chemical communications (Cambridge, England) 20050514
Properties