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C31600

Sigma-Aldrich

4-Chlorocinnamic acid

99%

Synonym(s):

trans-3-(4-Chlorophenyl)propenoic acid

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About This Item

Linear Formula:
ClC6H4CH=CHCO2H
CAS Number:
1615-02-7
Molecular Weight:
182.60
Beilstein:
2044025
EC Number:
216-564-8
MDL number:
MFCD00004396
UNSPSC Code:
12352100
PubChem Substance ID:
24892589
NACRES:
NA.22

Assay

99%

form

powder

mp

248-250 °C (lit.)

SMILES string

OC(=O)\C=C\c1ccc(Cl)cc1

InChI

1S/C9H7ClO2/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6H,(H,11,12)/b6-3+

InChI key

GXLIFJYFGMHYDY-ZZXKWVIFSA-N

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Marina Marinović et al.
Molecules (Basel, Switzerland), 25(19) (2020-09-27)
Harmicines represent hybrid compounds composed of β-carboline alkaloid harmine and cinnamic acid derivatives (CADs). In this paper we report the synthesis of amide-type harmicines and the evaluation of their biological activity. N-harmicines 5a-f and O-harmicines 6a-h were prepared by a
Ivana Perković et al.
European journal of medicinal chemistry, 187, 111927-111927 (2019-12-08)
Harmicines constitute novel hybrid compounds that combine two agents with reported antiplasmodial properties, namely β-carboline harmine and a cinnamic acid derivative (CAD). Cu(I) catalyzed azide-alkyne cycloaddition was employed for the preparation of three classes of hybrid molecules: N-harmicines 6a-i, O-harmicines

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