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Details

Stereochemistry ABSOLUTE
Molecular Formula C5H13NO
Molecular Weight 103.1628
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Valinol, L-

SMILES

CC(C)[C@H](N)CO

InChI

InChIKey=NWYYWIJOWOLJNR-RXMQYKEDSA-N
InChI=1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m1/s1

HIDE SMILES / InChI

Molecular Formula C5H13NO
Molecular Weight 103.1628
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
The Bogorol family of antibiotics: template-based structure elucidation and a new approach to positioning enantiomeric pairs of amino acids.
2006 Aug 4
Invariom-model refinement of L-valinol.
2006 Nov
Polymeric sulfated amino acid surfactants: a class of versatile chiral selectors for micellar electrokinetic chromatography (MEKC) and MEKC-MS.
2007 Feb 1
Amino acid derivatives from Lucilia sericata excretions/secretions may contribute to the beneficial effects of maggot therapy via increased angiogenesis.
2010 Mar
Synthesis of chiral β-aminoalcohol palladium complexes exhibiting cytotoxic properties.
2010 Oct 14
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 11:46:36 GMT 2023
Edited
by admin
on Sat Dec 16 11:46:36 GMT 2023
Record UNII
R54N4NJ3ZZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Valinol, L-
Common Name English
[(S)-1-(Hydroxymethyl)-2-methylpropyl]amine
Systematic Name English
1-Butanol, 2-amino-3-methyl-, (2S)-
Systematic Name English
L-VALINOL
Systematic Name English
1-Butanol, 2-amino-3-methyl-, L-
Systematic Name English
(S)-Valinol
Common Name English
NSC-322922
Code English
(2S)-2-Amino-3-methyl-1-butanol
Systematic Name English
(+)-Valinol
Common Name English
(+)-(S)-Valinol
Common Name English
(S)-(+)-2-Amino-3-methyl-1-butanol
Systematic Name English
Code System Code Type Description
CAS
2026-48-4
Created by admin on Sat Dec 16 11:46:36 GMT 2023 , Edited by admin on Sat Dec 16 11:46:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID901318132
Created by admin on Sat Dec 16 11:46:36 GMT 2023 , Edited by admin on Sat Dec 16 11:46:36 GMT 2023
PRIMARY
PUBCHEM
640993
Created by admin on Sat Dec 16 11:46:36 GMT 2023 , Edited by admin on Sat Dec 16 11:46:36 GMT 2023
PRIMARY
DRUG BANK
DB04383
Created by admin on Sat Dec 16 11:46:36 GMT 2023 , Edited by admin on Sat Dec 16 11:46:36 GMT 2023
PRIMARY
FDA UNII
R54N4NJ3ZZ
Created by admin on Sat Dec 16 11:46:36 GMT 2023 , Edited by admin on Sat Dec 16 11:46:36 GMT 2023
PRIMARY
ECHA (EC/EINECS)
217-975-5
Created by admin on Sat Dec 16 11:46:36 GMT 2023 , Edited by admin on Sat Dec 16 11:46:36 GMT 2023
PRIMARY
NSC
322922
Created by admin on Sat Dec 16 11:46:36 GMT 2023 , Edited by admin on Sat Dec 16 11:46:36 GMT 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
SALT/SOLVATE -> PARENT