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15369 Aldrich

N-Boc-ethylenediamine

≥98.0% (NT)

Synonym: N-Boc-1,2-diaminoethane, tert-Butyl N-(2-aminoethyl)carbamate

  • CAS Number 57260-73-8

  • Linear Formula (CH3)3COCONHCH2CH2NH2

  • Molecular Weight 160.21

  •  Beilstein Registry Number 1932330

  •  MDL number MFCD00191871

  •  PubChem Substance ID 57647392

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Properties

Related Categories Bifunctional Linkers, Building Blocks, Chemical Biology, Chemical Synthesis, Linkers and Crosslinkers,
InChI Key   AOCSUUGBCMTKJH-UHFFFAOYSA-N
assay   ≥98.0% (NT)
refractive index   n20/D 1.458(lit.)
  n20/D 1.458
bp   72-80 °C/0.1 mmHg(lit.)
density   1.012 g/mL at 20 °C(lit.)

Description

Other Notes

Mono-protected derivative of ethylenediamine, preparation of pharmacologically active analogues; introduction of an ethylenediamine spacer.

Packaging

1, 5, 25 g in glass bottle

Price and Availability


Cross-Coupling Guide
Safety & Documentation

Safety Information

Symbol 
GHS05  GHS05
Signal word 
Danger
Hazard statements 
Precautionary statements 
RIDADR 
UN 2735PSN1 8 / PGIII
WGK Germany 
3
Flash Point(F) 
235.4 °F
Flash Point(C) 
113 °C
Protocols & Articles

Articles

MRT - Ring Expansion

Potentially hazardous reagents like diazo compounds can be handled safely in microreactors because actual reaction volumes are very small. In a procedure developed at Johnson&Johnson ethyl diazoaceta...
Matthias Junkers
Aldrich ChemFiles 2009, 9.4, 13.
Keywords: Catalog, Chemfiles, Condensations, Continuous flow chemistry, Decarboxylations, Dieckmann Condensation, Michael Addition, Microreactor technology, Ring expansion

Mono-Protected Diaminoalkanes

Mono-Boc-protected diaminoalkanes are very useful for the introduction of homobifunctional spacers in many different applications. Additionally, they play an important role as building blocks in the ...
ChemFiles Volume 3 Article 4
Keywords: Applications, Building blocks

Peer-Reviewed Papers
15

References

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