Identification | More | [Name]
2-Chlorocinnamic acid | [CAS]
3752-25-8 | [Synonyms]
2-CHLOROCINNAMIC ACID (2E)-3-(2-CHLOROPHENYL)ACRYLIC ACID 3-(2-CHLORO-PHENYL)-ACRYLIC ACID 3-(2-CHLOROPHENYL)PROPENOIC ACID AKOS B004073 AKOS BBB/195 AKOS BBS-00006452 O-CHLOROCINNAMIC ACID OTAVA-BB BB0125160239 RARECHEM BK HC T319 (2E)-3-(2-Chlorophenyl)-2-propenoic acid 2-Propenoic acid, 3-(2-chlorophenyl)- 3-(2-chlorophenyl)-2-propenoicaci 3-(2-chlorophenyl)-2-propenoicacid Cinnamic acid, o-chloro- o-chloro-cinnamicaci 2-Chlorocinnamic acid, predominantly trans Chlorocinnamicacid 2-CHLOROCINNAMIC ACID, 99%, PREDOMINANTL Y TRANS 2-CLOROCINNAMIC ACID | [EINECS(EC#)]
223-154-2 | [Molecular Formula]
C9H7ClO2 | [MDL Number]
MFCD00004372 | [Molecular Weight]
182.6 | [MOL File]
3752-25-8.mol |
Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powder | [Melting point ]
208-210 °C(lit.)
| [Boiling point ]
260.71°C (rough estimate) | [density ]
1.2377 (rough estimate) | [refractive index ]
1.5426 (estimate) | [storage temp. ]
Room temperature. | [solubility ]
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | [Water Solubility ]
Insoluble in water | [form ]
powder to crystal | [pka]
4.23(at 25℃) | [color ]
White to Almost white | [BRN ]
1365198 | [InChIKey]
KJRRTHHNKJBVBO-AATRIKPKSA-N | [CAS DataBase Reference]
3752-25-8(CAS DataBase Reference) | [NIST Chemistry Reference]
2-Chlorocinnamic acid(3752-25-8) |
Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S36:Wear suitable protective clothing . S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [RTECS ]
GD8450000
| [Hazard Note ]
Irritant | [HS Code ]
29124990 |
Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystal powder | [Uses]
2-Chlorocinnamic acid is a kind of trans-cinnamate. It is used in organic synthesis. | [Biological Functions]
2-Chlorocinnamic acid is a cinnamic acid derivative that inhibits the hydroxylation of phenylpropanoids. It has been shown to inhibit the activity of cinnamic acid derivatives and their hydroxylation in cell lines, which is linked to the inhibition of cellulose acetate synthesis. 2-Chlorocinnamic acid also has an inhibitory effect on the chloride ion and water molecule. The chloride ion may be needed for the formation of hydrochloric acid, which is necessary for cellulose acetate hydrolysis, while water molecules are involved in many biochemical reactions. 2-Chlorocinnamic acid affects human cell lines at temperatures between 10°C and 37°C and at regiospecific sites. This oxidative dehalogenation reaction catalyzed by R. rubra was found to be regiospecific for 2-chlorocinnamic acid; the chloride ion was probably removed after the ring fission reaction. | [Synthesis]
O-chlorocinnamic acid is prepared by reacting o-phthalaldehyde with malonic acid. |
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