Boc-D-Homoser-OH

Boc-D-Homoser-OH - Names and Identifiers

Name	D-Homoserine,N-[(1,1-dimethylethoxy)carbonyl]-
Synonyms	Boc-D-homoserine Boc-D-Homoser-OH N-Boc-D-homoserine 4-Pyrimidinol,2-methoxy-7-methyl- (tert-Butoxycarbonyl)-D-homoserine D-Homoserine,N-[(1,1-dimethylethoxy)carbonyl]- D-Homoserine, N-[(1,1-dimethylethoxy)carbonyl]- D-Homoserine, N-[(1,1-dimethylethoxy)carbonyl]- (9CI) (R)-2-((tert-Butoxycarbonyl)amino)-4-hydroxybutanoicacid (2R)-2-{[(tert-butoxy)carbonyl]amino}-4-hydroxybutanoic acid
CAS	745011-75-0

Boc-D-Homoser-OH - Physico-chemical Properties

Molecular Formula	C9H17NO5
Molar Mass	219.24
Density	1.204±0.06 g/cm3(Predicted)
Boling Point	421.6±40.0 °C(Predicted)
pKa	3.87±0.10(Predicted)
Storage Condition	Sealed in dry,Room Temperature

Boc-D-Homoser-OH - Introduction

D-Homoserine,N-[(1,1-dimenthylethoxy) carbonyl]-is a chemical substance whose chemical name is D-Homoserine,N-[(1,1-dimenthylethoxy) carbonyl]-. The following is a detailed description of the nature, use, preparation and safety information of the substance:

Nature:
D-Homoserine,N-[(1,1-dimenthylethoxy) carbonyl]-is a white crystalline solid that is stable at room temperature. Its relative molecular mass is 209.25g/mol. This substance is soluble in anhydrous ether and insoluble in water.

Use:
D-Homoserine,N-[(1,1-dimenthylethoxy) carbonyl]-is commonly used as a substrate or intermediate in organic synthesis. It can participate in a variety of reactions, for example for the synthesis of biologically active compounds.

Preparation Method:
Generally, D-Homoserine,N-[(1,1-dimenthylethoxy) carbonyl]-can be synthesized through a two-step reaction. First, D-homoserine is reacted with 1,1-dimethyloxycarbonyl chloride (also known as Boc-Cl) to generate the Boc protecting group of D-Homoserine,N-[(1,1-dimethyllethoxy) carbonyl]. Then, the desired product is obtained by crystallization or column chromatography.

Safety Information:
When using or handling D-Homoserine,N-[(1,1-dimenthylethoxy) carbonyl]-, general laboratory safety procedures should be followed. It may be irritating to the eyes, skin and respiratory tract. Therefore, appropriate personal protective equipment, such as lab gloves, safety glasses and protective masks, should be worn. Anyone who comes into contact with the substance at work should maintain good ventilation and avoid direct inhalation of its powder or solution. If ingested or other accidents occur, seek medical attention immediately.

Last Update：2024-04-09 21:01:54