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Details

Stereochemistry RACEMIC
Molecular Formula C6H10O
Molecular Weight 98.143
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,5-HEXADIEN-3-OL

SMILES

OC(CC=C)C=C

InChI

InChIKey=SZYLTIUVWARXOO-UHFFFAOYSA-N
InChI=1S/C6H10O/c1-3-5-6(7)4-2/h3-4,6-7H,1-2,5H2

HIDE SMILES / InChI

Molecular Formula C6H10O
Molecular Weight 98.143
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Regioselective cross-metathesis reaction induced by steric hindrance.
2004-09-30
Enantioselective total synthesis of (+)-rogioloxepane A.
2003-08-21
Concerted rearrangement versus heterolytic cleavage in anionic [2,3]- and [3,3]-sigmatropic shifts. A DFT study of relationships among anion stabilities, mechanisms, and rates.
2003-03-21
The anionic oxy-Cope rearrangement: using chemical reactivity to reveal the facile isomerization of the parent substrates in the gas phase.
2001-11-02
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:12:25 GMT 2025
Edited
by admin
on Mon Mar 31 23:12:25 GMT 2025
Record UNII
C38864PH9K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,5-HEXADIEN-3-OL
Systematic Name English
NSC-102761
Preferred Name English
3-HYDROXY-1,5-HEXADIENE
Systematic Name English
1,5-HEXADIENE-3-OL
Systematic Name English
Code System Code Type Description
PUBCHEM
79122
Created by admin on Mon Mar 31 23:12:25 GMT 2025 , Edited by admin on Mon Mar 31 23:12:25 GMT 2025
PRIMARY
FDA UNII
C38864PH9K
Created by admin on Mon Mar 31 23:12:25 GMT 2025 , Edited by admin on Mon Mar 31 23:12:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID6022135
Created by admin on Mon Mar 31 23:12:25 GMT 2025 , Edited by admin on Mon Mar 31 23:12:25 GMT 2025
PRIMARY
CAS
924-41-4
Created by admin on Mon Mar 31 23:12:25 GMT 2025 , Edited by admin on Mon Mar 31 23:12:25 GMT 2025
PRIMARY
NSC
102761
Created by admin on Mon Mar 31 23:12:25 GMT 2025 , Edited by admin on Mon Mar 31 23:12:25 GMT 2025
PRIMARY
ECHA (EC/EINECS)
213-102-7
Created by admin on Mon Mar 31 23:12:25 GMT 2025 , Edited by admin on Mon Mar 31 23:12:25 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE