Passa al contenuto
Merck
Tutte le immagini(1)

Documenti

C81004

Sigma-Aldrich

Cinnamonitrile

97%

Sinonimo/i:

3-Phenylacrylonitrile

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

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

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

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)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 2

1 of 2

Hexanenitrile 98%

Sigma-Aldrich

166650

Hexanenitrile

Allyl cyanide 98%

Sigma-Aldrich

122793

Allyl cyanide

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
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
A J Alexander et al.
Analytical chemistry, 78(11), 3835-3838 (2006-06-02)
A directly coupled achiral/chiral SFC/MS method has been developed for the profiling of a three-step stereoselective synthesis of cinnamonitrile and hydrocinnamonitrile intermediates. Semipurified reaction mixtures were screened in one step to determine the diastereomeric/enantiomeric composition of the final product as
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
Visualizza tutti i documenti correlati

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.