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Home Sulfos Pyrrolidine-1-sulfonamide

Pyrrolidine-1-sulfonamide

CAS No.:
4108-88-7
Catalog Number:
AG00378J
Molecular Formula:
C4H10N2O2S
Molecular Weight:
150.1994
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
250mg
98%
In Stock USA
United States
$100
- +
1g
98%
In Stock USA
United States
$250
- +
5g
98%
In Stock USA
United States
$750
- +
10g
98%
In Stock USA
United States
$1200
- +
25g
98%
In Stock USA
United States
$2350
- +
Product Description
Catalog Number:
AG00378J
Chemical Name:
Pyrrolidine-1-sulfonamide
CAS Number:
4108-88-7
Molecular Formula:
C4H10N2O2S
Molecular Weight:
150.1994
MDL Number:
MFCD11171672
IUPAC Name:
pyrrolidine-1-sulfonamide
InChI:
InChI=1S/C4H10N2O2S/c5-9(7,8)6-3-1-2-4-6/h1-4H2,(H2,5,7,8)
InChI Key:
LPPOVVJDAVMOET-UHFFFAOYSA-N
SMILES:
NS(=O)(=O)N1CCCC1
Properties
Complexity:
175  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
150.046g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
150.196g/mol
Monoisotopic Mass:
150.046g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
71.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.7  
Literature
Title Journal
Pyrrolidinyl-sulfamide derivatives as a new class of bifunctional organocatalysts for direct asymmetric Michael addition of cyclohexanone to nitroalkenes. Organic & biomolecular chemistry 20110721
Structures of the class D carbapenemase OXA-24 from Acinetobacter baumannii in complex with doripenem. Journal of molecular biology 20110304
Tandem conjugate addition-elimination reaction promoted by chiral pyrrolidinyl sulfonamide (CPS). Chemical communications (Cambridge, England) 20081121
Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water. Organic letters 20080320
Design, synthesis, and evaluation of tetrahydroquinoline and pyrrolidine sulfonamide carbamates as gamma-secretase inhibitors. Bioorganic & medicinal chemistry letters 20070601
Enantio- and diastereoselective Michael addition reactions of unmodified aldehydes and ketones with nitroolefins catalyzed by a pyrrolidine sulfonamide. Chemistry (Weinheim an der Bergstrasse, Germany) 20060524
Properties