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Documenti

C80857

Sigma-Aldrich

trans-Cinnamic acid

≥99%

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
ID PubChem:
24893022
NACRES:
NA.22

Saggio

≥99%

Forma fisica

crystals

P. eboll.

300 °C (lit.)

Punto di fusione

132-135 °C (lit.)

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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Categorie correlate

Applicazioni

trans-Cinnamic acid can be used in the synthesis of:
  • A trans-cinnamic acid hydrazide derivative with potent anti-mycobacterial activity.
  • Cinnamate glycerides via homogeneous esterification reaction.
  • Styrene via biocatalytic decarboxylation by plant cell cultures.

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

Certificati d'analisi (COA)

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Methyl trans-cinnamate 99%

Sigma-Aldrich

173282

Methyl trans-cinnamate

p-Coumaric acid ≥98.0% (HPLC)

Sigma-Aldrich

C9008

p-Coumaric acid

trans-Cinnamic-d7 acid 98 atom % D

Sigma-Aldrich

513954

trans-Cinnamic-d7 acid

Urea 8 M (after reconstitution with 16 mL high purity water)

Supelco

U4883

Urea

Bromina reagent grade

Sigma-Aldrich

207888

Bromina

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

Synthesis and antimycobacterial evaluation of new trans-cinnamic acid hydrazide derivatives.
Carvalho SA, et al.
Bioorganic & Medicinal Chemistry, 18(2), 538-541 (2008)
Homogeneous catalytic esterification of glycerol with cinnamic and methoxycinnamic acids to cinnamate glycerides in solventless medium: Kinetic modeling.
Molinero L, et al.
Chemical Engineering Journal, 247(2), 174-182 (2014)
M Takemoto et al.
Chemical & pharmaceutical bulletin, 49(5), 639-641 (2001-06-01)
A novel method for producing styrenes from trans-cinnamic acids was developed. When trans-cinnamic acid was incubated with plant cell cultures at room temperature, styrene was obtained. 4-Hydroxy-3-methoxystyrene (2a), 3-nitrostyrene (2f) and furan (2g) were synthesized quantitatively.
Feng Yang et al.
Molecular pharmaceutics, 9(11), 3259-3265 (2012-09-27)
Owing to advantageous biochemical and pharmacological properties of human serum albumin (HSA), HSA-based drug carrier is playing an increasing role in the clinical setting. Since the IIA subdomain of HSA is a big hydrophobic cavity, we proposed that HSA delivers
Andrew M Lauer et al.
Organic letters, 14(19), 5138-5141 (2012-09-25)
A highly regioselective, Pd-catalyzed allylic fluorination of phosphorothioate esters is reported. This chemistry addresses several limitations of previously reported methods in which elimination and lack of reactivity were problematic. Preliminary mechanistic investigations reveal that these reactions are stereospecific and provide
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