ChemicalBook Product Catalog Organic Chemistry Amides Amino compound TERT-BUTYL N-(BENZYLOXY)CARBAMATE

TERT-BUTYL N-(BENZYLOXY)CARBAMATE

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
TERT-BUTYL N-(BENZYLOXY)CARBAMATE Structure
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
InChIKeyMZNBNPWFHGWAGH-UHFFFAOYSA-N
CAS DataBase Reference79722-21-7
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 29280000
MSDS Information
ProviderLanguage
SigmaAldrich English
TERT-BUTYL N-(BENZYLOXY)CARBAMATE Usage And Synthesis
Chemical PropertiesWhite powder
Usestert-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).
Usestert-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 Descriptiontert-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.
TERT-BUTYL N-(2-HYDROXYETHYL)CARBAMATE TERT-BUTYL N-(TERT-BUTOXYCARBONYLOXY)CARBAMATE O-(4-NITROBENZYL)HYDROXYLAMINE HYDROCHLORIDE TERT-BUTYL N-(BENZYLOXY)CARBAMATE N-BOC-3-(4-CYANOPHENYL)OXAZIRIDINE N-Hydroxyurethane RARECHEM AL BO 1195 ETHYL N-METHOXYCARBAMATE tert-Butyl N-hydroxycarbamate
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