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Details

Stereochemistry ACHIRAL
Molecular Formula C6H10
Molecular Weight 82.1436
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of 1,4-HEXADIENE, (4Z)-

SMILES

C\C=C/CC=C

InChI

InChIKey=PRBHEGAFLDMLAL-XQRVVYSFSA-N
InChI=1S/C6H10/c1-3-5-6-4-2/h3-4,6H,1,5H2,2H3/b6-4-

HIDE SMILES / InChI

Molecular Formula C6H10
Molecular Weight 82.1436
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A pinoresinol-lariciresinol reductase homologue from the creosote bush (Larrea tridentata) catalyzes the efficient in vitro conversion of p-coumaryl/coniferyl alcohol esters into the allylphenols chavicol/eugenol, but not the propenylphenols p-anol/isoeugenol.
2007-09-01
Addition of the phenoxathiin cation radical to alkenes and nonconjugated dienes. Formation of (E)- and (Z)-(10-phenoxathiiniumyl)alkenes and (E)- and (Z)-(10-phenoxathiiniumyl)dienes on basic alumina.
2007-08-03
A versatile hexadiene synthesis by decarboxylative sp(3)-sp(3) coupling/cope rearrangement.
2006-07-24
Ionizing radiation-induced destruction of benzene and dienes in aqueous media.
2006-05-01
New, abridged pathway to Masamune's "southern hemisphere" intermediate for the total synthesis of bryostatin 7.
2003-02-20
Facile allylic C-H bond activation on the bridging disulfide ligand in the Ru(III) dinuclear complex having a conjugated RuSSRu core.
2001-10-22
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:16:57 GMT 2025
Edited
by admin
on Mon Mar 31 21:16:57 GMT 2025
Record UNII
FUZ7TAA620
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(Z)-1,4-HEXADIENE
Preferred Name English
1,4-HEXADIENE, (4Z)-
Systematic Name English
1,4-CIS-HEXADIENE
Systematic Name English
1,4-HEXADIENE, (Z)-
Systematic Name English
CIS-1,4-HEXADIENE
Systematic Name English
NSC-157585
Code English
Code System Code Type Description
ECHA (EC/EINECS)
230-783-6
Created by admin on Mon Mar 31 21:16:57 GMT 2025 , Edited by admin on Mon Mar 31 21:16:57 GMT 2025
PRIMARY
EPA CompTox
DTXSID301015940
Created by admin on Mon Mar 31 21:16:57 GMT 2025 , Edited by admin on Mon Mar 31 21:16:57 GMT 2025
PRIMARY
NSC
157585
Created by admin on Mon Mar 31 21:16:57 GMT 2025 , Edited by admin on Mon Mar 31 21:16:57 GMT 2025
PRIMARY
CAS
7318-67-4
Created by admin on Mon Mar 31 21:16:57 GMT 2025 , Edited by admin on Mon Mar 31 21:16:57 GMT 2025
PRIMARY
PUBCHEM
5365553
Created by admin on Mon Mar 31 21:16:57 GMT 2025 , Edited by admin on Mon Mar 31 21:16:57 GMT 2025
PRIMARY
FDA UNII
FUZ7TAA620
Created by admin on Mon Mar 31 21:16:57 GMT 2025 , Edited by admin on Mon Mar 31 21:16:57 GMT 2025
PRIMARY