Skip to Content
Merck
All Photos(1)

Documents

C81004

Sigma-Aldrich

Cinnamonitrile

97%

Synonym(s):

3-Phenylacrylonitrile

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H5CH=CHCN
CAS Number:
1885-38-7
Molecular Weight:
129.16
Beilstein:
1209546
EC Number:
217-552-5
MDL number:
MFCD00001930
UNSPSC Code:
12352100
PubChem Substance ID:
24893023
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.601 (lit.)

bp

254-255 °C (lit.)

mp

18-20 °C (lit.)

density

1.028 g/mL at 25 °C (lit.)

SMILES string

N#C\C=C\c1ccccc1

InChI

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

InChI key

ZWKNLRXFUTWSOY-QPJJXVBHSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

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
Susanne Günther et al.
Journal of microbiological methods, 70(2), 272-283 (2007-06-15)
Cultivated bacterial toluene degraders use one or several of four described pathways for the aerobic degradation of this priority groundwater contaminant. To be able to identify un-cultivated toluene-degrading bacteria within enriched or natural consortia, we attempted to develop a set
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service