CHRYSANTHEMIC ACID, CIS-(+)-

CC(C)=C[C@H]1[C@@H](C(O)=O)C1(C)C

InChIKey=XLOPRKKSAJMMEW-YUMQZZPRSA-N

InChI=1S/C10H16O2/c1-6(2)5-7-8(9(11)12)10(7,3)4/h5,7-8H,1-4H3,(H,11,12)/t7-,8-/m0/s1

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

PubMed

Title	Date	PubMed
p1,n1 salts: Self-assembled supramolecular structures sequestering racemates. Diastereomeric separation and enantiomeric enrichment of trans-chrysanthemic acid.	2006 Nov 4	17047845
The racemate cage. Influence of p(1),n(1) salt occurrence on enantiomer separation processes. The case of trans-chrysanthemic acid.	2007 Jul 14	17594031
Characteristics and function of Alcaligenes sp. NBRC 14130 esterase catalysing the stereo-selective hydrolysis of ethyl chrysanthemate.	2010 Apr	19778353

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 05:27:32 GMT 2023` Edited by `admin` on `Sat Dec 16 05:27:32 GMT 2023`
Record UNII	5P7V8620AM
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

CHRYSANTHEMIC ACID, CIS-(+)-

Common Name

English

CYCLOPROPANECARBOXYLIC ACID, 2,2-DIMETHYL-3-(2-METHYL-1-PROPEN-1-YL)-, (1R,3S)-

Common Name

English

CYCLOPROPANECARBOXYLIC ACID, 2,2-DIMETHYL-3-(2-METHYL-1-PROPENYL)-, (1R,3S)-

Common Name

English

CHRYSANTHEMIC ACID D-CIS-FORM

Common Name

English

CIS-(+)-CHRYSANTHEMIC ACID

Common Name

English

Code System Code Type Description

ECHA (EC/EINECS)

247-996-5