PERILLALDEHYDE, (+)-

CC(=C)[C@@H]1CCC(C=O)=CC1

InChIKey=RUMOYJJNUMEFDD-JTQLQIEISA-N

InChI=1S/C10H14O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,7,10H,1,4-6H2,2H3/t10-/m0/s1

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

PubMed

Title	Date	PubMed
Site-saturation mutagenesis of tryptophan 116 of Saccharomyces pastorianus old yellow enzyme uncovers stereocomplementary variants.	2009-03-11	19226127
Opposite stereochemical courses for enzyme-mediated alkene reductions of an enantiomeric substrate pair.	2008-06-18	18500801
Parectadial, a monoterpenoid from the defensive spray of Parectatosoma mocquerysi.	2007-08	17661519

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:02:54 GMT 2025` Edited by `admin` on `Mon Mar 31 22:02:54 GMT 2025`
Record UNII	H5VW56IL2T
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

(+)-PERILLALDEHYDE

Preferred Name

English

PERILLALDEHYDE, (+)-

Common Name

English

(R)-(+)-PERILLALDEHYDE

Common Name

English

(R)-4-(PROP-1-EN-2-YL)CYCLOHEX-1-ENE-1-CARBOXALDEHYDE

Systematic Name

English

PERILLALDEHYDE D-FORM [MI]

Common Name

English

1-CYCLOHEXENE-1-CARBOXALDEHYDE, 4-(1-METHYLETHENYL)-, (4R)-

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID30364288