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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

Approval Year

PubMed

PubMed

TitleDatePubMed
A long-range chiral relay via tertiary amide group in asymmetric catalysis: new amino acid-derived N,P-ligands for copper-catalysed conjugate addition.
2003 Aug 7
Dietary low-dose sucrose modulation of IQ-induced genotoxicity in the colon and liver of Big Blue rats.
2003 Jun 19
Identification of a novel system L amino acid transporter structurally distinct from heterodimeric amino acid transporters.
2003 Oct 31
Asymmetric synthesis of 2-(2-pyridyl)aziridines from 2-pyridineimines bearing stereogenic N-alkyl substituents and regioselective opening of the aziridine ring.
2006 Dec 8
Vicinal amino alcohols as organocatalysts in asymmetric cross-aldol reaction of ketones: application in the synthesis of convolutamydine A.
2007 Dec 20
β-Amino alcohol selectors for enantioselective separation of amino acids by ligand-exchange capillary zone electrophoresis in a low molecular weight organogel.
2010 Dec
Synthesis of chiral β-aminoalcohol palladium complexes exhibiting cytotoxic properties.
2010 Oct 14
Patents
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
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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
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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
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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
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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
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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
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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
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