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133760

Sigma-Aldrich

trans-Cinnamic acid

97%

Sinonimo/i:

trans-3-Phenylacrylic acid, Cinnamic acid

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About This Item

Formula condensata:
C6H5CH=CHCOOH
Numero CAS:
140-10-3
Peso molecolare:
148.16
Beilstein:
1905952
Numero CE:
205-398-1
Numero MDL:
MFCD00004369
Codice UNSPSC:
12352100
eCl@ss:
39023931
ID PubChem:
24848120
NACRES:
NA.22
Stato:
solid
Saggio:
97%

Livello qualitativo

200

Saggio

97%

Stato

solid

P. ebollizione

300 °C (lit.)

Punto di fusione

132-135 °C (lit.)

Gruppo funzionale

carboxylic acid
phenyl

Stringa SMILE

OC(=O)\C=C\c1ccccc1

InChI

1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+
WBYWAXJHAXSJNI-VOTSOKGWSA-N

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Applicazioni

trans-Cinnamic acid was used to establish library of phenolic compounds by liquid chromatography/ultraviolet and mass spectrometry/mass spectrometry.

Azioni biochim/fisiol

trans-cinnamic acid has inhibitory effect on phorbol-12-myristate-13-acetate-induced invasion of human lung adenocarcinoma A549 cells. It is a potential agent which can prevent lung tumor cells from metastasizing. It induces intracellular release of Ca2+ from the vacuole to the cytoplasm which triggers phytotoxicity in cucumber.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H319

Classi di pericolo

Eye Irrit. 2

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

320.0 °F - closed cup

Punto d’infiammabilità (°C)

160 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
MKCT2411
0000207856
MKCQ9252
MKCP8118
MKCN6727

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2,3-DIBROMO-3-PHENYLPROPIONIC ACID AldrichCPR

S764841

2,3-DIBROMO-3-PHENYLPROPIONIC ACID

trans-Stilbene 96%

Sigma-Aldrich

139939

trans-Stilbene

Acetanilide 99%

Sigma-Aldrich

112933

Acetanilide

trans-Cinnamic acid-β,2,3,4,5,6-d6 98 atom % D

Sigma-Aldrich

513962

trans-Cinnamic acid-β,2,3,4,5,6-d6

Methyl cinnamate ≥99.0% (GC)

Sigma-Aldrich

96410

Methyl cinnamate

Methyl trans-cinnamate 99%

Sigma-Aldrich

173282

Methyl trans-cinnamate

Jingquan Yu et al.
Journal of chemical ecology, 35(12), 1471-1477 (2010-01-12)
To obtain insight into interspecies interactions mediated by allelochemicals, the response of cucumber (Cucumis sativus L. cv Jinyan No.4) and figleaf gourd (Cucurbita ficifolia Bouché) seedlings to trans-cinnamic acid (CA) (1) was investigated. While trans-CA is an autotoxin in cucumber
Chiung-Man Tsai et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 48(3), 494-501 (2012-12-12)
Dietary polyphenols have been reported as an effective phytochemical for health protection and cinnamic acid (CA) is one of the polyphenols that has been demonstrated having chemopreventive potential. It was known that the early and distal metastasis might lead to
Barbara Speranza et al.
Microorganisms, 8(6) (2020-06-25)
Twelve fungal strains were assayed to investigate their resistance to cinnamic and vanillic acids and their ability to remove these compounds from a liquid medium. In a first step, the effect of the two aromatic acids (1 g/L) on the
Jianping Sun et al.
Molecules (Basel, Switzerland), 12(3), 679-693 (2007-09-14)
Liquid chromatography/ultraviolet (LC/UV) and mass spectrometry/mass spectrometry (MS/MS) libraries containing 39 phenolic compounds were established by coupling a LC and an ion trap MS with an electrospray ionization (ESI) source, operated in negative ion mode. As a result, the deprotonated
Bianca C Pérez et al.
Journal of medicinal chemistry, 56(2), 556-567 (2013-01-01)
The control of malaria is challenged by drug resistance, and new antimalarial drugs are needed. New drug discovery efforts include consideration of hybrid compounds as potential multitarget antimalarials. Previous work from our group has demonstrated that hybrid structures resulting from
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