Identification | More | [Name]
3-Chlorocinnamic acid | [CAS]
1866-38-2 | [Synonyms]
(2E)-3-(3-CHLOROPHENYL)ACRYLIC ACID 3-CHLOROCINNAMIC ACID AKOS BBS-00006453 AURORA 22720 (E)-3-(3-CHLOROPHENYL)ACRYLIC ACID M-CHLOROCINNAMIC ACID RARECHEM BK HC T320 (2E)-3-(3-Chlorophenyl)-2-propenoic acid 2-Propenoic acid, 3-(3-chlorophenyl)- Cinnamic acid, m-chloro- trans-3-Chlorocinnamic acid (2E)-3-(3-chlorophenyl)prop-2-enoic acid 3-CHLOROCINNAMIC ACID, 98%, PREDOMINANTL Y TRANS 3-Chlorocinnamic acid, 98+% 3-Chlorocinnamic acid, predominantly trans, 99+% 3-chlorocinnamic acid, predominantly trans 3-Chlorocinnamic acid 98% 3-CHLOROCINNAMIC ACID, PREDOMINANTLY TRANS, 98+% 3-Chlorocinnamic acid trans-3-(3-Chlorophenyl)propenoic acid | [EINECS(EC#)]
217-478-3 | [Molecular Formula]
C9H7ClO2 | [MDL Number]
MFCD00004384 | [Molecular Weight]
182.6 | [MOL File]
1866-38-2.mol |
Safety Data | Back Directory | [Hazard Codes ]
Xi,Xn | [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 ]
S22:Do not breathe dust . S24/25:Avoid contact with skin and eyes . 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
| [Hazard Note ]
Irritant | [TSCA ]
Yes | [HS Code ]
29163990 |
Hazard Information | Back Directory | [Chemical Properties]
white crystalline powder or crystals | [Synthesis]
GENERAL METHOD: Under stirring conditions, 6.76 g (65 mmol) of malonic acid was dissolved in a mixed solution of 5 mL of pyridine and 0.5 mL of piperidine. Subsequently, 3-chlorobenzaldehyde (50 mmol) was slowly added at 85°C. The reaction mixture was stirred continuously for 6 hours, during which the progress of the reaction was monitored by thin layer chromatography (TLC) to confirm complete consumption of the feedstock. Upon completion of the reaction, the mixture was cooled to room temperature and neutralized with 10% hydrochloric acid solution under ice bath conditions, at which point a white solid was observed to precipitate. The solid product was collected by filtration and washed three times with ice water to remove impurities. Finally, the target product 3-chlorocinnamic acid (2a-h) was obtained by recrystallization and purification using aqueous ethanol (1:1, v/v). | [References]
[1] Journal of Organic Chemistry, 2009, vol. 74, # 23, p. 9152 - 9157 [2] Journal of Chemical Research, 2005, # 6, p. 364 - 365 [3] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 7, p. 1849 - 1853 [4] Proceedings - Indian Academy of Sciences, Section A, 1941, vol. 14, p. 116 - 120 [5] Chem.Abstr., 1942, p. 1599 |
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