2-((tert-Butoxycarbonyl)amino)-3-ethoxy-3-oxopropanoic Acid CAS 137401-45-7

We can provide 2-((tert-Butoxycarbonyl)amino)-3-ethoxy-3-oxopropanoic acid CAS 137401-45-7 with a certificate of analysis (COA), method of analysis (MOA), route of synthesis (ROS), and material safety data sheet (MSDS)

 

Chemical Properties：

Density:1.2±0.1 g/cm3

Index of Refraction:1.470

Boiling point: 397.2±37.0 °C at 760 mmHg

Flash Point:194.0±26.5 °C

 

Synonyms：

Ethyl tert-Butoxycarbonyl-DL-aminomalonate

N-Boc-2-amino-3-ethoxy-3-oxopropanoic Acid

2-(N-BOC-AMINO)MALONIC ACID MONOETHYL ESTER

2-[N-(tert-butoxy)forMaMido]-3-ethoxy-3-oxopropanoic acid

2-((tert-Butoxycarbonyl)aMino)-3-ethoxy-3-oxopropanoic acid

3-ethoxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-oxopropanoic acid

Propanedioic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, 1-ethyl ester

 

2-((tert-Butoxycarbonyl)amino)-3-ethoxy-3-oxopropanoic acid CAS 137401-45-7 has a wide range of uses in organic synthesis, including the following:

As a chemical reagent: 2-((tert-Butoxycarbonyl)amino)-3-ethoxy-3-oxopropanoic acid CAS 137401-45-7 can be used as a reagent in organic synthesis reactions, such as a carboxylic acid protection reagent in carboxylic acid carboxylate synthesis, which protects the carboxylic acid functional group.

Research compounds: 2-tert-butoxycarbonylamino can also be used in chemistry-related experiments and research to explore new synthetic methods and reactions.

 

The preparation of 2-tert-butoxycarbonylamino can be generally obtained by the following steps:

Reacting dipropyl 2-aminomalonate with N-tert-butoxycarbonylcarbohydrazide to form dipropyl 2-(N-BOC-AMINO)malonate.

Reaction of dipropyl 2-(N-BOC-AMINO)malonate with sodium hypochlorite to form 2-(N-BOC-AMINO)malonic acid.

2-(N-BOC-AMINO)malonic acid is reacted with ethanol to form 2-tert-butoxycarbonylamino.

This compound may be irritating to the eyes and skin, avoid contact with unprotected skin and eyes.

When handling and manipulating, it is necessary to do so in a well-ventilated area and wear appropriate personal protective equipment such as laboratory gloves, protective eyewear, and a lab coat.

Avoid inhaling or ingesting the compound, avoid generating dust and follow proper laboratory safety procedures.

When disposing of waste, it should be disposed of in strict accordance with local regulations to avoid contamination of the environment.

 

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