ethylenediamine, n-benzyl-

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Names

[ CAS No. ]:
4152-09-4

[ Name ]:
ethylenediamine, n-benzyl-

[Synonym ]:
N-benzylethane-1,2-diamine
ethylenediamine, n-benzyl-
N'-benzylethane-1,2-diamine
N-Benzyl-1,2-ethanediamine
1,2-Ethanediamine, N-(phenylmethyl)-
N1-Benzylethane-1,2-diamine
EINECS 223-984-5
MFCD00041896

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
259.5±15.0 °C at 760 mmHg

[ Molecular Formula ]:
C9H14N2

[ Molecular Weight ]:
150.221

[ Flash Point ]:
127.6±24.0 °C

[ Exact Mass ]:
150.115692

[ PSA ]:
38.05000

[ LogP ]:
0.84

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.542

[ Water Solubility ]:
negligible

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S23-S26-S36/37/39-S45

[ RIDADR ]:
2735

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
2921590090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2921590090

[ Summary ]:
2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

An anionic nucleophilic catalyst system for the diastereoselective synthesis of trans-beta-lactams.

Org. Lett. 7(16) , 3461-3, (2005)

Trans-disubstituted beta-lactams show increasing utility and prominence in numerous pharmaceutical applications, making their asymmetric synthesis an attractive goal for chemists. We introduce an anio...

A new method for the synthesis of tri-tert-butyl diethylenetriaminepentaacetic acid and its derivatives. Achilefu S, et al.

J. Org. Chem. 65(5) , 1562-1565, (2000)

Application of a-chloroaldoxime O-methanesulfonates to one-pot synthesis of N, N', N?-substituted guanidines via Tiemann rearrangement. Yamamoto Y, et al.

Tetrahedron Lett. 50(42) , 5813-5815, (2009)


More Articles

Related Compounds

  • benzyl-(2-chloroethyl)-[2-(diethylamino)ethyl]azanium,chloride
  • 1,2-Ethanediamine,N1,N2-dioctyl-
  • N'-benzyl-N,N-dimethyl-N'-naphthalen-1-ylethane-1,2-diamine
  • Hydrazinium,1-acetyl-2,2-dimethyl-2-(phenylmethyl)-, chloride (1:1)
  • (ethylenediamine-N,N')bis(nitrito-N)palladium
  • Ethylenediamine-N,N''-disuccinic acid
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • Methyl[2-(pyrazin-2-yl)propan-2-yl]amine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide