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5-(t-Butyloxycarbonyl-aMino)-3-oxapentanoic acid

Acetic acid, [2-[[(1,1-dimethylethoxy)carbonyl]amino]ethoxy]-

CAS: 142929-49-5

Molecular Formula: C9H17NO5

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  5. 5-(t-Butyloxycarbonyl-aMino)-3-oxapentanoic acid

5-(t-Butyloxycarbonyl-aMino)-3-oxapentanoic acid - Names and Identifiers

Name Acetic acid, [2-[[(1,1-dimethylethoxy)carbonyl]amino]ethoxy]-
Synonyms DCHA
Boc-O1Pen-OH*DCHA
t-Boc-N-amido-PEG1-CH2CO2H
(2-Boc-Aminoethoxy)acetic acid
Boc-5-Amino-3-oxapentanoic acid
5-(t-Butyloxycarbonyl-aMino)-3-oxapentanoic acid
{2-[(tert-butoxycarbonyl)amino]ethoxy}acetic acid
2-(2-((tert-Butoxycarbonyl)aMino)ethoxy)acetic acid
5-[[(tert-Butoxy)carbonyl]amino]-3-oxapentanoic acid
Acetic acid, [2-[[(1,1-dimethylethoxy)carbonyl]amino]ethoxy]-
Acetic acid, [2-[[(1,1-dimethylethoxy)carbonyl]amino]ethoxy]- (9CI)
5-(t-Butyloxycarbonyl-amino)-3-oxapentanoic acid, [2-(Boc-amino)ethoxy]acetic acid, dicyclohexylamine
CAS 142929-49-5
InChI InChI=1/C9H17NO5/c1-9(2,3)15-8(13)10-4-5-14-6-7(11)12/h4-6H2,1-3H3,(H,10,13)(H,11,12)

5-(t-Butyloxycarbonyl-aMino)-3-oxapentanoic acid - Physico-chemical Properties

Molecular FormulaC9H17NO5
Molar Mass219.24
Density1.151±0.06 g/cm3(Predicted)
Boling Point391.2±22.0 °C(Predicted)
Flash Point190.4°C
Vapor Presure3.3E-07mmHg at 25°C
pKa3.44±0.10(Predicted)
Storage Condition-20°C
Refractive Index1.462

5-(t-Butyloxycarbonyl-aMino)-3-oxapentanoic acid - Introduction

Boc-5, also known as Boc-GABA-OH, is an organic compound. The following is a description of its nature, use, preparation and safety information:

Nature:
Boc-5-Amino -3-oxopentanoic acid is a colorless crystalline solid with the formula C10H19NO5. It has moderate solubility and is soluble in some common organic solvents. It is a neutral compound that is relatively stable under normal storage conditions.

Use:
Boc-5-amino -3-oxopentanoic acid is commonly used in the field of drug synthesis. It can be used as an intermediate of GABA receptor modulators for the synthesis of some biologically active molecules. It can also be used as a protecting group in organic synthesis.

Preparation Method:
The synthesis of Boc-5-amino -3-oxopentanoic acid is generally completed by organic synthesis reaction. A common preparation method is to obtain Boc-5-amino-3-oxopentanoic acid by introducing a Boc protecting group (tert-butoxycarbonyl) into the GABA molecule, followed by an oxidation reaction.

Safety Information:
Regarding the safety of Boc-5-amino -3-oxopentanoic acid, first of all, care should be taken to avoid direct contact with skin, eyes or inhalation of its dust. Care should be taken to wear appropriate personal protective equipment such as chemical protective gloves and safety glasses during use. In addition, any chemical should be used under safe and ventilated conditions and stored in a dry, sealed and dark place.

In general, Boc-5-amino -3-oxopentanoic acid is a useful organic synthesis intermediate, but it is necessary to follow relevant safety procedures when using and handling it to ensure the safety of laboratory operations.
Last Update:2024-04-09 20:52:54
5-(t-Butyloxycarbonyl-aMino)-3-oxapentanoic acid
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