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Details

Stereochemistry ABSOLUTE
Molecular Formula C4H11N
Molecular Weight 73.1368
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-BUTANAMINE, (S)-

SMILES

CC[C@H](C)N

InChI

InChIKey=BHRZNVHARXXAHW-BYPYZUCNSA-N
InChI=1S/C4H11N/c1-3-4(2)5/h4H,3,5H2,1-2H3/t4-/m0/s1

HIDE SMILES / InChI

Molecular Formula C4H11N
Molecular Weight 73.1368
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparison of the omega-transaminases from different microorganisms and application to production of chiral amines.
2001 Aug
Novel modified adenosine 5'-triphosphate analogues pharmacologically characterized in human embryonic kidney 293 cells highly expressing rat brain P2Y(1) receptor: Biotinylated analogue potentially suitable for specific P2Y(1) receptor isolation.
2001 May 15
Discovery of 8-hydroxyadenines as a novel type of interferon inducer.
2002 Dec 5
The effect of ligand charge on the coordination geometry of an Fe(III)ion: five- and six-coordinate Fe(III) complexes of tris(2-benzimidazolylmethyl)amine.
2002 Sep 9
Substitution reactions of 5-nitropyridine-2-sulfonic acid. A new pathway to 2,5-disubstituted pyridines.
2003 Aug 7
Microbial synthesis of (R)- and (S)-3,4-dimethoxyamphetamines through stereoselective transamination.
2003 Nov
DNA interactions of new antitumor platinum complexes with trans geometry activated by a 2-metylbutylamine or sec-butylamine ligand.
2004 Mar 15
Kinetic resolution of (R,S)-sec-butylamine using omega-transaminase from Vibrio fluvialis JS17 under reduced pressure.
2004 Sep 20
Chiral recognition by resorcin[4]arene receptors: intrinsic kinetics and dynamics.
2004 Sep 6
Synthesis and in vitro skin permeation of naproxen conjugates with alpha-alkylamino acids.
2005 Apr
Microbial synthesis of chiral amines by (R)-specific transamination with Arthrobacter sp. KNK168.
2006 Jan
Gas-phase enantioselectivity of chiral amido[4]resorcinarene receptors.
2006 Oct 25
Efficacy of a novel biofilter in hatchery sanitation: II. Removal of odorogenous pollutants.
2007
Review of sitagliptin phosphate: a novel treatment for type 2 diabetes.
2007
Monosolvation of R-1-phenyl-2,2,2-trifluoroethanol with amines: configurational effects on the excitation, ionization, and fragmentation of diastereomeric complexes.
2007 Dec 13
Modelling amphetamine/receptor interactions: a gas-phase study of complexes formed between amphetamine and Some chiral amido[4]resorcinarenes.
2008
Induced-fit in the gas phase: conformational effects on the enantioselectivity of chiral tetra-amide macrocycles.
2008 Jan 16
A kinetic study of guest displacement reactions on a host-guest complex with a photoswitchable calixarene.
2008 Nov
Enantiomerically pure quaternary ammonium salts with a chiral alkyl chain N(CH3)(n-C3H7)2(sec-C4H9)I: synthesis and physical studies.
2008 Nov
4-{(Z)-(sec-Butyl-amino)(phen-yl)methyl-ene}-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one.
2009 Aug 8
Peripheral blood monocytes are responsible for gammadelta T cell activation induced by zoledronic acid through accumulation of IPP/DMAPP.
2009 Jan
Interaction of antitumor platinum complexes with human liver microsomal cytochromes P450.
2009 Jun
A functional gammadeltaTCR/CD3 complex distinct from gammadeltaT cells is expressed by human eosinophils.
2009 Jun 17
Inhibition of protein kinase C-driven nuclear factor-kappaB activation: synthesis, structure-activity relationship, and pharmacological profiling of pathway specific benzimidazole probe molecules.
2010 Jun 24
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:17:56 GMT 2023
Edited
by admin
on Fri Dec 15 15:17:56 GMT 2023
Record UNII
Z192XWH21O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-BUTANAMINE, (S)-
Systematic Name English
SEC-BUTYLAMINE D-FORM [MI]
Common Name English
SEC-BUTYLAMINE, (S)
Common Name English
(2S)-BUTANAMINE
Common Name English
(S)-SEC-BUTYLAMINE
Systematic Name English
SEC-BUTYLAMINE D-FORM
MI  
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID00883416
Created by admin on Fri Dec 15 15:17:56 GMT 2023 , Edited by admin on Fri Dec 15 15:17:56 GMT 2023
PRIMARY
FDA UNII
Z192XWH21O
Created by admin on Fri Dec 15 15:17:56 GMT 2023 , Edited by admin on Fri Dec 15 15:17:56 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-164-7
Created by admin on Fri Dec 15 15:17:56 GMT 2023 , Edited by admin on Fri Dec 15 15:17:56 GMT 2023
PRIMARY
MERCK INDEX
m2816
Created by admin on Fri Dec 15 15:17:56 GMT 2023 , Edited by admin on Fri Dec 15 15:17:56 GMT 2023
PRIMARY Merck Index
CAS
513-49-5
Created by admin on Fri Dec 15 15:17:56 GMT 2023 , Edited by admin on Fri Dec 15 15:17:56 GMT 2023
PRIMARY
PUBCHEM
6713753
Created by admin on Fri Dec 15 15:17:56 GMT 2023 , Edited by admin on Fri Dec 15 15:17:56 GMT 2023
PRIMARY