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ChemicalBook--->CAS DataBase List--->90940-40-2

90940-40-2

90940-40-2 Structure

90940-40-2 Structure
IdentificationBack Directory
[Name]

2-(4-CHLORO-PHENYL)-CYCLOPROPANECARBOXYLIC ACID
[CAS]

90940-40-2
[Synonyms]

NSC 40845
AKOS B006809
2-(4-Chlorophenyl)
ART-CHEM-BB B006809
2-(4-CHLORO-PHENYL)-CYCLOPROPANECARBOXYLIC ACID
2-(4-chlorophenyl)cyclopropane-1-carboxylic acid
Cyclopropanecarboxylic acid, 2-(4-chlorophenyl)-
trans-2-(4-chlorophenyl)cyclopropane-1-carboxylic acid
[Molecular Formula]

C10H9ClO2
[MDL Number]

MFCD03419437
[MOL File]

90940-40-2.mol
[Molecular Weight]

196.63
Chemical PropertiesBack Directory
[Melting point ]

112 °C
[Boiling point ]

346.9±42.0 °C(Predicted)
[density ]

1.388±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

4.53±0.10(Predicted)
[Appearance]

White to off-white Solid
[Optical Rotation]

0.1°(C=0.46g/ml, CHCL3 , 20°C, 589nm)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[Hazard Codes ]

Xi,T
[Risk Statements ]

25
[Safety Statements ]

45
[HazardClass ]

IRRITANT
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

2-(4-CHLORO-PHENYL)-CYCLOPROPANECARBOXYLIC ACID(90940-40-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Cyclopropanecarboxylic acid, 2-(4-chlorophenyl)-, ethyl ester, (1R,2S)-rel-

4103-56-4

trans-2-(4-Chloro-phenyl)-cyclopropanecarboxylic acid

4157-47-5

GENERAL METHOD: 1 g of NaOH (25 mmol) was dissolved in 4 cm3 of a solvent mixture of EtOH/H?O (85/15; v/v) and cooled to the appropriate temperature. Subsequently, 9 cm3 EtOH solution containing ester 18-20 (2.21 mmol) was added. The reaction mixture was stirred continuously for 5 hours at room temperature. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in 30 cm3 water and the aqueous layer was washed with 2 x 15 cm3 CH?Cl? The aqueous layer was subsequently acidified with concentrated HCl and extracted with 3 x 15 cm3 CH?Cl? All organic layers were combined, dried with Na?SO? and finally evaporated to dryness.

[References]

[1] Monatshefte fur Chemie, 2017, vol. 148, # 12, p. 2143 - 2153
[2] Bulletin de la Societe Chimique de France, 1960, p. 304 - 312
[3] Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1957, vol. 245, p. 2304
[4] Bulletin de la Societe Chimique de France, 1960, p. 304,307, 308
[5] Bulletin de la Societe Chimique de France, 1960, p. 304 - 312
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