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TERT-BUTYL N-(BENZYLOXY)CARBAMATE

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TERT-BUTYL N-(BENZYLOXY)CARBAMATE Basic information

Product Name:
TERT-BUTYL N-(BENZYLOXY)CARBAMATE
Synonyms:
  • LABOTEST-BB LT00452293
  • TERT-BUTYL N-(BENZYLOXY)CARBAMATE
  • N-(BENZYLOXY)CARBAMIC ACID TERT-BUTYL ESTER
  • N-Boc-O-benzylhydroxylamine
  • TERT-BUTYL BENZYLOXYCARBAMATE
  • O-Benzylhydroxylamine, N-BOC protected, tert-Butyl (phenylmethoxy)carbamate
  • tert-Butyl (benzyloxy)carbamate 99%
  • tert-Butyl N-(benzyloxy)carbamate ,98%
CAS:
79722-21-7
MF:
C12H17NO3
MW:
223.27
EINECS:
628-800-0
Product Categories:
  • Hydroxylamines
  • Hydroxylamines (N-Substituted)
  • Hydroxylamines (O-Substituted)
  • Nitrogen Compounds
  • Organic Building Blocks
  • Protected Amines
Mol File:
79722-21-7.mol
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TERT-BUTYL N-(BENZYLOXY)CARBAMATE Chemical Properties

Melting point:
45-47 °C (lit.)
Density 
1.078±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
form 
Solid
color 
White
InChIKey
MZNBNPWFHGWAGH-UHFFFAOYSA-N
CAS DataBase Reference
79722-21-7
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29280000

MSDS

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TERT-BUTYL N-(BENZYLOXY)CARBAMATE Usage And Synthesis

Chemical Properties

White powder

Uses

tert-Butyl N-(benzyloxy)carbamate was used in the preparation of seven-membered cyclic hydroxamic acids. It may be used in the synthesis of 2-(N-formyl-N-hydroxyamino) ethylphosphonate (IPP).

Uses

tert-Butyl N-(Benzyloxy)carbamate has been used in the synthesis of Deferoxamine Mesylate (D228980), an iron chelating agent used in therapy for patients with sickle cell diseases and iron overload. Studies suggest that it can exert potential antioxidant neuroprotective effects in stroke patients

General Description

tert-Butyl N-(benzyloxy)carbamate (tert-butyl benzyloxycarbamate), a protected hydroxylamine, is an N-alkyl-N-benzyloxy carbamate. Its C-N cross coupling reaction with fluorescein ditriflate has been reported. It participates in facile intramolecular cyclization with various carbon nucleophiles to afford functionalized 5- and 6-membered protected cyclic hydroxamic acids.

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