Benzenepropanenitrile

HCID 12581

Basic information

CAS
645-59-0
Standard SMILES
N#CCCc1ccccc1
InChIKey
ACRWYXSKEHUQDB-UHFFFAOYSA-N
Molecular formula
C9H9N
Average molar mass
131.17 g/mol
Monoisotopic mass
131.07349929

Overview

3-phenylpropionitrile is a nitrile that is propionitrile in which one of the methyl hydrogens has been replaced by a phenyl group. It is a nitrile and a member of benzenes. It is functionally related to an acetonitrile.

Names & identifiers

Preferred name
Benzenepropanenitrile
IUPAC
3-phenylpropanenitrile
English name
3-PHENYLPROPIONITRILE
Molecular formula
C9H9N
Molecular weight
131.17

Names & synonyms

3-PhenylpropionitrileBenzenepropanenitrile3-Phenylpropiononitrile1-Cyano-2-phenylethaneUNII-H2Y1JYN13QEINECS 211-447-8H2Y1JYN13QBRN 0636348AI3-23733beta-phenylpropionitrileNSC-16936DTXSID4060949
Show more names
3-PhenylpropanenitrileHYDROCINNAMONITRILEBenzenepropionitrileNSC 16936phenethylcyanidePhenethyl cyanideBenzylacetonitrilePhenylpropionitrile2-Phenylethylcyanide
CHEBI:854264-09-00-01764 (Beilstein Handbook Reference)b-Phenylethyl cyanideb-Phenyl propionitrileRefChem:117692DTXCID8044333ACRWYXSKEHUQDB-UHFFFAOYSA-NInChI=1/C9H9N/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6H,4,7H

Database identifiers

CAS
645-59-0
PubChem CID
12581
DTXSID
DTXSID4060949
ChEBI
CHEBI:85426
UNII
H2Y1JYN13Q
EC Number
211-447-8
Nikkaji
J45.903H

Properties

Computed structural properties

XLogP
1.7
Topological polar surface area
23.8 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
1
Rotatable bonds
2
Heavy atoms
10

Experimental & physicochemical properties

SpringerMaterials PropertiesChemical shift
LogP · 2 items

1.72

1.72

Boiling Point261.00 °C. @ 760.00 mm Hg
Melting Point-1 °C
Physical DescriptionLiquid

Physicochemical properties

Melting point
2 · −2-−1 °C(lit.)
Boiling point
113 °C9 · 113 °C9 mm Hg(lit.)
Density
1.001 g/mL · 1.001 g/mL at 25 °C(lit.)
refractive index
20 · n20/D 1.521(lit.)
Flash point
230 °F · >230 °F
storage temp.
Sealed in dry,Room Temperature

Safety & regulation

GHS classification

GHS Classification · 4 items

Danger

H301 (80.7%): Toxic if swallowed [Danger Acute toxicity, oral]

P261, P262, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P302+P352, P304+P340, P305+P351+P338, P316, P319, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 57 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Hazard Classes and CategoriesAcute Tox. 3 (80.7%)

Safety data

PPE
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
wgk
3
tsca
TSCA listed
rtecs
MW5604750
ridadr
UN 3276 6.1/PG 3
hs_code
29269095

Chemistry & industry

Pharmacology

Cellular LocationsCytoplasm

Uses & manufacturing

General Manufacturing InformationBenzenepropanenitrile: INACTIVE
Applications · 3 items

Uses3-Phenylpropionitrile was used to study the free enzyme activity of nitrilase AtNIT1.

UsesA glucosinolate enzymic hydrolosis product with potential antibacterial activities against plant pathogenic bacteria. 3-Phenylpropionitrile is occasionally used in perfume compositions, mainly as a minor ingredient in artificial flower absolutes, etc. The material can also be used in certain types of exotic or very heavy floral fragrance, e. g. Stephanotis, Pikake, Keora, Ginger Lily, Tiare, Coffee flower, etc. Its warm and piquant, vegetable pungency is utilized in flavor compositions for seasonings, etc. and in various spice blends. Normal use concentration is equivalent to about 1 to 3 ppm in the finished product.

General DescriptionThe effect of 3-Phenylpropionitrile on the growth and survival of woodlouse Porcellio scaber has been studied.

Preparation methods · 1 item

PreparationTo a stirred solution of 3-phenylpropanamide (50 mg, 0.34 mmol) in acetonitrile (0.8 mL) at room temperature were successively added formic acid (0.2 mL) and paraformaldehyde (50 mg, 1.67 mmol). The reaction mixture was then refluxed for 12 h, and the solution obtained was cooled to room temperature. Work-up A: The crude mixture was concentrated under reduced pressure, and the residue was subjected to flash chromatography on silica gel (230–240 mesh) eluting with hexane/ethyl acetate (7:3) to yield 3-phenylpropanonitrile (37 mg, 85%). Work-up B: The reaction mixture was diluted with ethyl acetate (10 mL) and washed successively with saturated sodium hydrogen carbonate solution (5 mL) and water (5 mL). The combined aqueous layers were extracted with ethyl acetate (2 × 10 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated. The crude 3-phenylpropanonitrile was purified as described above (Work-up A).

Upstream & downstream products

Suppliers67 total

梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
Hebei Chuanghai Biotechnology Co., Ltd+86-17732866630 · [email protected]
上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
Dayang Chem (Hangzhou) Co.,Ltd.+86-0571-88938639 17705817739 · [email protected]
淮安嘉目生物科技有限公司0517-83187139 18205232085 · [email protected]

Additional notes

DefinitionChEBI: A nitrile that is propionitrile in which one of the methyl hydrogens has been replaced by a phenyl group.

Related reactions

12 records

Compound notes

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