4,4-Dimethoxybutanenitrile

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Names

[ Name ]:
4,4-Dimethoxybutanenitrile

[Synonym ]:
4,4-Dimethoxybutyronitrile
4,4-Dimethoxybutanenitrile
EINECS 238-658-8
MFCD00019883
Butanenitrile, 4,4-dimethoxy-
3-Cyanopropionaldehyde dimethyl acetal
3-Cyanopropionaldehydedimethylacetal

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
201.4±30.0 °C at 760 mmHg

[ Molecular Formula ]:
C₆H₁₁NO₂

[ Molecular Weight ]:
129.157

[ Flash Point ]:
89.4±0.0 °C

[ Exact Mass ]:
129.078979

[ PSA ]:
42.25000

[ LogP ]:
-0.31

[ Vapour Pressure ]:
0.3±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.410

[ Storage condition ]:
2-8°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 ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
20/21/22

[ Safety Phrases ]:
S36

[ RIDADR ]:
3276

[ WGK Germany ]:
3

[ HS Code ]:
2926909090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2926909090

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

An easy access to 7-methyl-2-naphthalenecarbonitrile.

Chem. Pharm. Bull. 53(4) , 448-50, (2005)

A practical and cost-effective procedure has been developed for the synthesis of 7-methyl-2-naphthalenecarbonitrile, the precursor of the anticoagulant agents YM-60828 or YM-96765. This new route gene...

2-formyl-4,4-dimethoxybutanenitrile
2-formyl,4,4-dimethoxybutanenitrile
2-formyl,4,4-dimethoxybutanenitrile
4-(4-aminophenyl)-1,3-dihydroimidazol-2-one
4-(4-aminobutyl)phenol
4,4,5,5-tetramethyl-2-(1-phenylprop-1-enyl)-1,3,2-dioxaborolane
Tert-butyl 3,3-difluoro-[2,3'-biazetidine]-1'-carboxylate
2-(2-{[(Benzyloxy)carbonyl]amino}-5-chloro-1,3-thiazol-4-yl)-2,2-difluoroacetic acid
4-({[(Benzyloxy)carbonyl]amino}methyl)-1-methyl-2-oxabicyclo[2.1.1]hexane-3-carboxylic acid
{3-[(4-Acetylpiperazin-1-yl)methyl]phenyl}boronic acid
1-(2,3-dihydro-1H-isoindol-2-yl)-2-(methylamino)propan-1-one hydrochloride
2-(Oxolan-3-yloxy)pyridin-4-amine hydrochloride
8-Bromo-1,2,3,5-tetrahydro-4,1-benzothiazepine hydrochloride
4,4'-Bis((8-amino-1-hydroxy-5,7-disulfo-2-naphthalenyl)diazenyl)[biphenyl]-3,3'-dicarboxylic acid
azane;[(2R,3R)-2-[(2,2-dichloroacetyl)amino]-3-hydroxy-3-(4-nitrophenyl)propyl] hexadecanoate
C.I. Direct Red 28, compd. with 1,a3-adimethyl-a1,a3-adiphenylguanidine (1:2)

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