Peperacetonitrile

Suppliers

Names

[ Name ]:
Peperacetonitrile

[Synonym ]:
2-(1,3-benzodioxol-5-yl)acetonitrile
3,4-Methylenedioxybenzyl Cyanide
EINECS 224-655-9
3,4-Methylenedioxyphenylacetonitrile
Homopiperonylonitrile
Peperacetonitrile
MFCD00005835
1,3-Benzodioxol-5-ylacetonitrile
1,3-Benzodioxole-5-acetonitrile
2-(Benzo[d][1,3]dioxol-5-yl)acetonitrile
2-(Benzo[d][1,3]dioxol-6-yl)acetic acid

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
299.7±9.0 °C at 760 mmHg

[ Melting Point ]:
43-45 °C(lit.)

[ Molecular Formula ]:
C₉H₇NO₂

[ Molecular Weight ]:
161.157

[ Flash Point ]:
130.5±11.9 °C

[ Exact Mass ]:
161.047684

[ PSA ]:
42.25000

[ LogP ]:
1.31

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.575

[ Storage condition ]:
0-10°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302 + H312 + H332

[ Precautionary Statements ]:
P280

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
S36-S36/37

[ RIDADR ]:
3439

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2932999099

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

Methylenedioxyphenethylamine
5-Bromo-1,3-benzodioxole
sodium cyanoacetate
Piperonyl alcohol
2-(benzo[d][1,3]dioxol-5-yl)-2-(methylthio)acetonitrile
POTASSIUM CYANIDE
MDBN
5-(Chloromethyl)-1,3-benzodioxole
Sodium cyanide

DownStream

1-BENZO[1,3]DIOXOL-5-YL-CYCLOPROPANECARBONITRILE
1,3-Benzodioxole-5-aceticacid, methyl ester
1,3-Benzodioxole-5-acetonitrile,a-formyl-
1-(BENZO[D][1,3]DIOXOL-5-YL)CYCLOPROPANECARBOXYLIC ACID
1,3-Benzodioxol-5-ylacetic acid
2-(2H-1,3-Benzodioxol-5-yl)acetamide
3,4-Methylenedioxytoluene
Methyl piperonyl ketone
1,3-Benzodioxole-5-ethanimidamide
7H-1,3-Dioxolo[4,5-g][2]benzopyran-7-one, 5,8-dihydro-

Customs

[ HS Code ]: 2932999099

[ Summary ]:
2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Synthesis and evaluation of derrubone and select analogues.

J. Org. Chem. 73(2) , 369-73, (2008)

Recently, we reported that the natural product derrubone exhibits Hsp90 inhibitory activity. Due to its unique architectural scaffold and proposed rapid assembly, the synthesis of this natural product...

Enzymatic nitrile hydrolysis catalyzed by nitrilase ZmNIT2 from maize. An unprecedented ß-hydroxy functionality enhanced amide formation. Mukherjee C, et al.

Tetrahedron 62(26) , 6150-54, (2006)

Seized methamphetamine samples with unique profiles of stable nitrogen isotopic composition documented by stable isotope ratio mass spectrometry. Iwata YT, et al.

Forensic Toxicol. 28(2) , 119-123, (2010)

N-((1-(3-fluorophenyl)-1H-tetrazol-5-yl)methyl)naphthalene-2-sulfonamide
3-chloro-N-((1-(3-fluorophenyl)-1H-tetrazol-5-yl)methyl)benzenesulfonamide
N-((1-(3-fluorophenyl)-1H-tetrazol-5-yl)methyl)-2-(trifluoromethyl)benzenesulfonamide
N-{[1-(4-chlorophenyl)-1H-1,2,3,4-tetrazol-5-yl]methyl}-4-fluorobenzene-1-sulfonamide
N-{[1-(4-chlorophenyl)-1H-1,2,3,4-tetrazol-5-yl]methyl}-2-fluorobenzene-1-sulfonamide
N-((1-(4-chlorophenyl)-1H-tetrazol-5-yl)methyl)-3-fluorobenzenesulfonamide
2-chloro-N-((1-(4-chlorophenyl)-1H-tetrazol-5-yl)methyl)benzenesulfonamide
N-((1-(4-chlorophenyl)-1H-tetrazol-5-yl)methyl)-2-(trifluoromethyl)benzenesulfonamide
N-((1-(4-chlorophenyl)-1H-tetrazol-5-yl)methyl)-3-(trifluoromethyl)benzenesulfonamide
N-{[1-(3,4-difluorophenyl)-1H-1,2,3,4-tetrazol-5-yl]methyl}benzenesulfonamide

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