Product

TERT-BUTYL N-(BENZYLOXY)CARBAMATE

CAS No.：79722-21-7

Other grades of this product :

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 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

Safety Information

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

MSDS Information

Provider	Language
SigmaAldrich	English

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.

TERT-BUTYL N-(BENZYLOXY)CARBAMATE Preparation Products And Raw materials

Raw materials

Dichloromethane-->N,N-Dimethylformamide-->Sodium carbonate-->Potassium carbonate-->Potassium hydroxide-->Sodium bicarbonate-->Acetonitrile-->Isopropyl alcohol-->Dimethyl sulfoxide-->Di-tert-butyl dicarbonate-->Hydrazine hydrate-->Benzyl chloride-->N,N-Diisopropylethylamine-->N-Hydroxyphthalimide

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