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C81004

Sigma-Aldrich

Cinnamonitrile

97%

Sinonimo/i:

3-Phenylacrylonitrile

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About This Item

Formula condensata:
C6H5CH=CHCN
Numero CAS:
1885-38-7
Peso molecolare:
129.16
Beilstein:
1209546
Numero CE:
217-552-5
Numero MDL:
MFCD00001930
Codice UNSPSC:
12352100
ID PubChem:
24893023
NACRES:
NA.22

Saggio

97%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.601 (lit.)

P. eboll.

254-255 °C (lit.)

Punto di fusione

18-20 °C (lit.)

Densità

1.028 g/mL at 25 °C (lit.)

Stringa SMILE

N#C\C=C\c1ccccc1

InChI

1S/C9H7N/c10-8-4-7-9-5-2-1-3-6-9/h1-7H/b7-4+
ZWKNLRXFUTWSOY-QPJJXVBHSA-N

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Pittogrammi

Skull and crossbones
GHS06

Avvertenze

Danger

Indicazioni di pericolo

H301

Classi di pericolo

Acute Tox. 3 Oral

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

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Sigma-Aldrich

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Sigma-Aldrich

122793

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Derek Fischer et al.
Nature protocols, 2(1), 227-236 (2007-04-03)
A procedure for the synthesis of a ratiometric viscosity fluorescent sensor is described in this protocol. The essential requirement for the design of this sensor is the attachment of a primary fluorophore that has both a viscosity-independent fluorescence emission (coumarin
P J van Bladeren et al.
Drug metabolism and disposition: the biological fate of chemicals, 9(3), 246-249 (1981-05-01)
After administration of acrylonitrile, crotononitrile and cinnamonitrile to rats, two types of mercapturic acids were isolated from urine and identified by mass and NMR spectroscopy as N-acetyl-S-(2-cyanoethyl)-L-cysteine (I) and N-acetyl-S-(2-hydroxyethyl)-L-cysteine (II) (methyl-substituted in the case of crotonitrile and phenyl-substituted in
Deepali N Mehta-Hurt et al.
The Journal of chemical physics, 143(7), 074304-074304 (2015-08-25)
In Titan's atmosphere, photochemical pathways that lead to nitrogen heteroaromatics may incorporate photoisomerization of their structural isomers as a final step. (E)- and (Z)-phenylvinylnitrile ((E)- and (Z)-PVN, C6H5-CH=CHCN) are structural isomers of quinoline that themselves possess extensive absorptions in the
Yasushi Obora et al.
Organic & biomolecular chemistry, 8(18), 4071-4073 (2010-07-24)
A facile direct synthesis of cinnamonitriles from acrylonitriles and benzenes is successfully achieved by using Pd(OAc)(2)/HPMoV/O(2) catalyst system via the direct C-H bond activation of benzenes using molecular oxygen as a terminal oxidant.
Iana M Serafimova et al.
Nature chemical biology, 8(5), 471-476 (2012-04-03)
Targeting noncatalytic cysteine residues with irreversible acrylamide-based inhibitors is a powerful approach for enhancing pharmacological potency and selectivity. Nevertheless, concerns about off-target modification motivate the development of reversible cysteine-targeting strategies. Here we show that electron-deficient olefins, including acrylamides, can be
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