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ethyl chrysanthemate, mixed isomers cis and trans

Ethyl chrysanthemumate, mixture of cis andtrans

CAS: 97-41-6

Molecular Formula: C12H20O2

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ethyl chrysanthemate, mixed isomers cis and trans - Names and Identifiers

Name Ethyl chrysanthemumate, mixture of cis andtrans
Synonyms Ethyl chrysanthemat
ETHYL CHRYSANTHEMATE
Ethyl chrysanthemate
ETHYL CHRYSANTHEMUMATE
Ethyl chrysanthemumate
Primary ethyl chrysanthemate
Chrysanthemic acid ethyl ester
Ethyl Chrysanthemate (Primary)
CHRYSANTHEMYLMONOCARBOXYLIC ACID ETHYL ESTER
chrysanthemum monocarboxylic acid ethyl ester
CHRYSANTHEMUM MONOCARBOXYLIC ACID ETHYL ESTER
Ethyl chrysanthemumate, mixture of cis andtrans
ethyl chrysanthemate, mixed isomers cis and trans
Ethyl 2,2-dimethyl-3-(1-isobutenyl)cyclopropane-1-carboxylate
ethyl 2,2-dimethyl-3-(2-methylpropenyl)cyclopropanecarboxylate
Ethyl 2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate
ethyl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate
2,2-DIMETHYL-3-(1-ISOBUTENYL)CYCLOPROPANE-1-CARBOXYLIC ACID ETHYL ESTER
ethyl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate
ethyl (1S,3S)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate
2,2-DIMETHYL-3-(2-METHYL-1-PROPENYL)CYCLOPROPANE CARBOXYLIC ACID ETHYL ESTER
ethyl (1R,3S)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate
ethyl (1S,3R)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate
ethyl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate
(1R,3S)-2,2-dimethyl-3-(2-methylprop-1-enyl)-1-cyclopropanecarboxylic acid ethyl ester
CAS 97-41-6
EINECS 202-579-7
InChI InChI=1/C12H20O2/c1-6-14-11(13)10-9(7-8(2)3)12(10,4)5/h7,9-10H,6H2,1-5H3/t9-,10-/m0/s1

ethyl chrysanthemate, mixed isomers cis and trans - Physico-chemical Properties

Molecular FormulaC12H20O2
Molar Mass196.29
Density0.906g/mLat 25°C(lit.)
Boling Point112°C10mm Hg(lit.)
Flash Point184°F
Solubility Chloroform (Slightly), Methanol (Slightly)
Vapor Presure0.0372mmHg at 25°C
AppearanceLiquid
ColorYellow
BRN2045740
Storage Condition2-8°C
Refractive Indexn20/D 1.461(lit.)
MDLMFCD00001304
Physical and Chemical Properties(+) ethyl cis-trans chrysanthemum acid is a colorless or light yellow oily liquid, B. p.112 ℃/1.33 kpa,n20D1.460, relative density 0.906,f.p.184 ℉(84 ℃). Insoluble in water, soluble in ethanol, methanol, acetone, benzene, toluene and other organic solvents.
UseIt is mainly used for the key intermediates of insecticides such as permethrin, cypermethrin, phenylethrin, and propermethrin.

ethyl chrysanthemate, mixed isomers cis and trans - Risk and Safety

Safety Description24/25 - Avoid contact with skin and eyes.
WGK Germany2
RTECSGZ1727000
TSCAYes
HS Code29162090

ethyl chrysanthemate, mixed isomers cis and trans - Reference Information

NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
Application The ethyl ester can be used as a pharmaceutical synthesis intermediate, such as the preparation of 6, 6-dimethyl-3-oxabicyclo [3.1.0] hexane -2, 4-dione, 6, 6-dimethyl-3-oxabicyclo [3.1.0] hexane -2, 4-dione is an important intermediate for the production of novel drugs targeting the hepatitis C Virus replication site.
Use ethyl pyrethrate is an important intermediate of pyrethroid, A variety of hygienic pyrethroids can be prepared.
hygienic intermediates
can be used as raw materials for organic synthesis, pharmaceutical intermediates
is an important intermediate for the preparation of permethrin and other pesticides
mainly used in the preparation of permethrin, key intermediates of insecticides, such as Phenothrin and prynthrin,
production method diazoacetate method 2, 5-dimethyl-2, 4-hexadiene was added to the reaction flask, with the amount of Diene 59/6 copper powder as catalyst, and then add a little hydroquinone as antioxidant, under nitrogen heating to 120 ℃, under rapid stirring, drop heavier methyl acetate solution, when dropping, N2 is released, and the reaction rate is controlled. After dropping, stirring is continued for 0.5h, cooling, and the excess Diene is removed by distillation, the recovered Diene can be recycled., Ethyl pyrethate was obtained by replacing methyl diazoacetate with ethyl diazoacetate.
Last Update:2024-04-09 20:49:11
ethyl chrysanthemate, mixed isomers cis and trans
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View History
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