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Details

Stereochemistry ABSOLUTE
Molecular Formula C5H13NO.ClH
Molecular Weight 139.624
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Valinol hydrochloride, L-

SMILES

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

InChI

InChIKey=CYONGLLQMUYOPP-NUBCRITNSA-N
InChI=1S/C5H13NO.ClH/c1-4(2)5(6)3-7;/h4-5,7H,3,6H2,1-2H3;1H/t5-;/m1./s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Sequences of polypeptide antibiotics stilboflavins, natural peptaibol libraries of the mold Stilbella flavipes.
2001 Aug
A total synthesis of (-)-hemiasterlin using N-Bts methodology.
2001 Nov 2
Invariom-model refinement of L-valinol.
2006 Nov
Molecular modeling of chiral-modified zeolite HY employed in enantioselective separation.
2007 Jun
Enantioseparation of phenylglycinol in chiral-modified zeolite HY: a molecular simulation study.
2007 Jun
Asymmetric synthesis of 8-aminoindolizidine from chiral 2-pyrroleimines.
2008 Nov 7
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 19:20:41 GMT 2023
Edited
by admin
on Sat Dec 16 19:20:41 GMT 2023
Record UNII
CSD9XWZ26Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Valinol hydrochloride, L-
Common Name English
1-Butanol, 2-amino-3-methyl-, hydrochloride, L-
Systematic Name English
1-Butanol, 2-amino-3-methyl-, hydrochloride (1:1), (2S)-
Systematic Name English
(S)-2-Amino-3-methylbutan-1-ol hydrochloride
Common Name English
1-Butanol, 2-amino-3-methyl-, hydrochloride, (S)-
Systematic Name English
(S)-Valinol hydrochloride
Common Name English
Code System Code Type Description
CAS
17016-89-6
Created by admin on Sat Dec 16 19:20:42 GMT 2023 , Edited by admin on Sat Dec 16 19:20:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID20647395
Created by admin on Sat Dec 16 19:20:42 GMT 2023 , Edited by admin on Sat Dec 16 19:20:42 GMT 2023
PRIMARY
PUBCHEM
24802562
Created by admin on Sat Dec 16 19:20:42 GMT 2023 , Edited by admin on Sat Dec 16 19:20:42 GMT 2023
PRIMARY
FDA UNII
CSD9XWZ26Q
Created by admin on Sat Dec 16 19:20:42 GMT 2023 , Edited by admin on Sat Dec 16 19:20:42 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE