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
Characteristics and function of Alcaligenes sp. NBRC 14130 esterase catalysing the stereo-selective hydrolysis of ethyl chrysanthemate.	2010-04	19778353
The racemate cage. Influence of p(1),n(1) salt occurrence on enantiomer separation processes. The case of trans-chrysanthemic acid.	2007-07-14	17594031
p1,n1 salts: Self-assembled supramolecular structures sequestering racemates. Diastereomeric separation and enantiomeric enrichment of trans-chrysanthemic acid.	2006-11-04	17047845

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:38:45 GMT 2025` Edited by `admin` on `Mon Mar 31 21:38:45 GMT 2025`
Record UNII	1J3B3RQ0Q8
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

CHRYSANTHEMIC ACID DL-CIS-FORM

Preferred Name

English

CHRYSANTHEMIC ACID, CIS-(±)-

Common Name

English

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

Common Name

English

CHRYSANTHEMIC ACID DL-CIS-FORM [MI]

Common Name

English

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

Common Name

English

(±)-CIS-CHRYSANTHEMIC ACID

Common Name

English

Code System Code Type Description

ECHA (EC/EINECS)

220-908-2