Benzyl (2-aminoethyl)carbamate | CAS No. 72080-83-2

Benzyl (2-aminoethyl)carbamate

Basic Information

CAS Number

72080-83-2

Molecular Formula

C10H14N2O2

Molecular Weight

194.23 g/mol

AD

Basic Physical Properties

Melting Point

169-172 °C

C1=CC=C(C=C1)COC(=O)NCCN

InChI

InChI=1S/C10H14N2O2/c11-6-7-12-10(13)14-8-9-4-2-1-3-5-9/h1-5H,6-8,11H2,(H,12,13)

InChIKey

QMMFTRJQCCVPCE-UHFFFAOYSA-N

LogP

0.8714999999999997

Topological Polar Surface Area

64.35 Ų

Hydrogen Bond Donor/Acceptor

3 / 4

Complexity

168

Synonyms & References

English

  • N-(2-aminoethyl)carbamic acid (phenylmethyl) ester
  • N-CBZ-1,2-DIAMINOETHANE
  • Carbamic acid, (2-aminoethyl)-, phenylmethyl ester
  • J-519772
  • N-1-Z-1,2-diaminoethane HCl
  • 72080-83-2
  • BP-31251
  • SCHEMBL614872
  • EN300-197440
  • Benzyl (2-aminoethyl)carbamate
  • DTXSID50383193
  • AKOS006230656
  • SY102986
  • 2-benzyloxycarbonylaminoethylamine
  • benzyl(2-aminoethyl)carbamate
  • A837416
  • N1-Cbz-1,2-ethanediamine
  • DS-16556
  • FT-0657023
  • N-1-Z-1,2-diaminoethane . HCl
  • MFCD02094510
  • benzyl 2-aminoethylcarbamate
  • N-CBZ-ETHYLENEDIAMINE
  • Carbamic acid,N-(2-aminoethyl)-, phenylmethyl ester
  • n-benzyloxycarbonyl-ethylenediamine
  • Benzyl 2-aminoethylcarbamate, AldrichCPR
  • (2-amino-ethyl)-carbamic acid benzyl ester
  • QMMFTRJQCCVPCE-UHFFFAOYSA-N
  • BB 0267117
  • Benzyl N-(2-aminoethyl)carbamate
  • A26808

MDL Number

MFCD02094510

Customs Code

2924299090

FAQ

What are the physical and chemical properties of Benzyl (2-aminoethyl)carbamate (CAS: 72080-83-2)?

Benzyl (2-aminoethyl)carbamate (CAS: 72080-83-2) is a white crystalline solid with a molecular weight of approximately 196.24 g/mol. It is slightly soluble in water and soluble in organic solvents like ethanol and acetone. This compound is known for its reactivity, particularly in nucleophilic substitution reactions and it is stable under normal conditions but should be handled with care due to its potential to form toxic byproducts.

How is Benzyl (2-aminoethyl)carbamate (CAS: 72080-83-2) typically synthesized?

Benzyl (2-aminoethyl)carbamate (CAS: 72080-83-2) is usually synthesized through the reaction of benzyl isothiocyanate with ethylene diamine. The process involves the condensation of these two reactants in the presence of a suitable catalyst at room temperature, leading to a high yield of the target compound. This method provides good selectivity and is often used in the production of this compound for various applications.

What industries use Benzyl (2-aminoethyl)carbamate (CAS: 72080-83-2)?

Benzyl (2-aminoethyl)carbamate (CAS: 72080-83-2) is primarily used in the pharmaceutical industry for the synthesis of drugs, particularly in the production of certain analgesics and antihistamines. It is also used in the polymer industry for the modification of polymers to enhance their properties. Additionally, it is utilized in the semiconductor industry for the fabrication of sensors and in the production of some electronic materials.

What precautions should be taken when handling Benzyl (2-aminoethyl)carbamate (CAS: 72080-83-2)?

When handling Benzyl (2-aminoethyl)carbamate (CAS: 72080-83-2), it is essential to wear appropriate personal protective equipment (PPE), including gloves, goggles, and a lab coat. This compound should be handled in a well-ventilated area or a fume hood to minimize exposure to fumes. Spills should be contained and cleaned up using appropriate methods, and the use of safety data sheets (SDS) is recommended for detailed handling and emergency response information.

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