38267-76-4

Basic information

• Product Name: N-Boc-ethylaMine, 97%
• Synonyms: N-Boc-ethylaMine, 97%;tert-Butyl N-ethylcarbaMate;tert-butyl ethylcarbaMate
• CAS NO: 38267-76-4
• Molecular Formula: C₇H₁₅NO₂
• Molecular Weight: 145
• Mol File: 38267-76-4.mol
• Article Data: 8

Chemical Properties

• Melting Point: 38-41℃
• Appearance: /
• Storage Temp.: 2-8°C
• Solubility: Dichloromethane, THF
• CAS DataBase Reference: N-Boc-ethylaMine, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: N-Boc-ethylaMine, 97%(38267-76-4)
• EPA Substance Registry System: N-Boc-ethylaMine, 97%(38267-76-4)

Safety Data

• Hazardous Substances Data: 38267-76-4(Hazardous Substances Data)

Usage

Uses

N-?Ethyl-?carbamic Acid 1,?1-?Dimethylethyl Ester is an intermediate in synthesizing Ethalfluralin (E917718), a herbicide.

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 36016-38-3 tert-Butyl N-hydroxycarbamate 
• 1310366-23-4 tert-butyl propionyloxycarbamate 
• 557-66-4 ethanamine hydrochloride 
• 557-20-0 diethylzinc 
• 462100-44-3 oxaziridine-2,3,3-tricarboxylic acid 2-tert-butyl ester 3,3-diethyl ester 
• 150884-56-3 N-tert-butyloxycarbonyl-3-(4-cyanophenyl)oxaziridine 
• 216959-34-1 ethyl 2-{[(tert-butoxy)carbonyl]amino}-2-oxoacetate 
• 4248-19-5 tert-butyl carbazate 
• 365441-85-6 N-(tert-butoxycarbonyl)-1-tosyleth-1-ylamine 
• 216959-38-5 (tert-butoxycarbonyl-ethyl-amino)-oxo-acetic acid ethyl ester 
• 41840-28-2 S-tert-butoxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine 
• 75-04-7 ethylamine 
• 507-40-4 tert-butylhypochlorite 

Downstream Products

• 120157-98-4 N-(tert-butyloxycarbonyl)glycine 

Relevant articles and documents

Deuterium-modified carbapenem derivatives

The invention belongs to the technical field of medicines, and particularly relates to deuterium-modified carbapenem derivatives or pharmaceutically acceptable salts thereof, a method for preparing the compounds, pharmaceutical preparations and pharmaceut

Base-Mediated Intramolecular Decarboxylative Synthesis of Alkylamines from Alkanoyloxycarbamates

A general and effective method for the synthesis of alkylamine via intramolecular decarboxylation of alkanoyloxycarbamates is described. The alkanoyloxycarbamates are readily prepared with alkyl carboxylic acids and hydroxylamine. The reaction shows a broad range of substrates (primary and secondary alkyl) with functional tolerance, and the corresponding products were obtained in good yields under mild conditions.

Electrophilic amination of diorganozinc reagents by oxaziridines

Electrophilic amination of organozinc reagents by oxaziridines has been studied. Diorganozinc reagents R2Zn (R = alkyl or aryl) react with N-Boc oxaziridine to afford N-Boc protected primary amines BocNHR in moderate to good yields. No additive