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Principaux documents

13300

Sigma-Aldrich

Phenylacetonitrile

purum, ≥98.0% (GC)

Synonyme(s) :

Benzyl cyanide

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About This Item

Formule linéaire :
C6H5CH2CN
Numéro CAS:
Poids moléculaire :
117.15
Beilstein:
385941
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
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Qualité

purum

Essai

≥98.0% (GC)

Indice de réfraction

n20/D 1.524

pb

231-233 °C (lit.)

Densité

1.015 g/mL at 20 °C (lit.)

Chaîne SMILES 

N#CCc1ccccc1

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Autres remarques

This product has been replaced by B19401-ALDRICH | Benzyl cyanide 98%
Sales restrictions may apply

Pictogrammes

Skull and crossbones

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 1 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

215.6 °F - closed cup

Point d'éclair (°C)

102 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Certificats d'analyse (COA)

Lot/Batch Number

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Magzoub O Bashir et al.
Journal of insect physiology, 56(6), 640-645 (2010-02-09)
Previous studies had demonstrated stage differentiation in the cohesion (aggregation) pheromone systems of the desert locust, Schistocerca gregaria. In laboratory arena, the nymphal and adult stages responded aggregatively to their own pheromone, but dispersed evenly within the arena in the
José Luis García Ruano et al.
The Journal of organic chemistry, 72(16), 5994-6005 (2007-07-17)
Enantiomerically pure alpha-substituted alpha-amino phenylacetonitriles have been readily prepared from 2-p-tolylsulfinylbenzaldimines following a two-step sequence: a moderately stereoselective hydrocyanation of the imines and a completely stereoselective quaternization of the resulting diastereoisomeric mixture of alpha-amino phenylacetonitriles with different alkylating or acylating
Liping Huang et al.
Organic letters, 14(24), 6122-6125 (2012-12-06)
A small organic molecule phenylacetonitrile promoted chemoselective cyclization of (chromen-3-yl)alkynylnitriles to generate a novel tetracyclic or tricyclic chromone scaffold has been discovered. Importantly, the phenylacetonitrile serves as an anion transfer reagent changing the normal reaction of the substrate.
Martinus E Huigens et al.
Journal of chemical ecology, 37(4), 364-367 (2011-04-01)
Males of a variety of insects transfer an anti-aphrodisiac pheromone to females during mating that renders them less attractive to conspecific males. In cabbage white butterflies, the transfer of an anti-aphrodisiac can result in the unwanted attraction of tiny egg
Jacques Corset et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(5), 1340-1346 (2007-05-01)
The carbanionic species possibly formed during the first alkylation step of phenylacetonitrile lithiated anion by CH(3)I and PhCH(2)Cl in THF-hexane solution and their complexes with the lithium salt formed have been observed by infrared spectrometry and characterized by density functional

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