N-[(2S)-2-吗啉基甲基]氨基甲酸叔丁酯

N-[(2S)-2-吗啉基甲基]氨基甲酸叔丁酯 - Names and Identifiers

Name	(S)-2-N-Boc-aminomethylmorpholine
Synonyms	(S)-2-N-Boc-aminomethylmorpholine (S)-2-(Boc-aMinoMethyl)Morpholine -tert-Butyl (morpholin-2-ylmethyl) tert-Butyl-[(2S)-morpholin-2-ylmethyl]carbamat (S)-tert-Butyl (Morpholin-2-ylMethyl)carbaMate tert-Butyl [(2S)-morpholin-2-ylmethyl]carbamate tert-butyl N-[(2S)-morpholin-2-ylmethyl]carbamate N-[(2S)-2-Morpholinylmethyl]carbamic acid 1,1-dimethylethyl ester Carbamic acid, N-[(2S)-2-morpholinylmethyl]-, 1,1-dimethylethyl ester carbamic acid, N-[(2S)-2-morpholinylmethyl]-, 1,1-dimethylethyl ester
CAS	875551-59-0
InChI	InChI=1/C10H20N2O3/c1-10(2,3)15-9(13)12-7-8-6-11-4-5-14-8/h8,11H,4-7H2,1-3H3,(H,12,13)/t8-/m0/s1

N-[(2S)-2-吗啉基甲基]氨基甲酸叔丁酯 - Physico-chemical Properties

Molecular Formula	C10H20N2O3
Molar Mass	216.28
Density	1.032±0.06 g/cm3(Predicted)
Boling Point	334.0±17.0 °C(Predicted)
Flash Point	155.8°C
Vapor Presure	0.000131mmHg at 25°C
pKa	12.22±0.46(Predicted)
Storage Condition	2-8°C(protect from light)
Refractive Index	1.452

N-[(2S)-2-吗啉基甲基]氨基甲酸叔丁酯 - Introduction

(S)-is an organic compound with the chemical formula C11H21NO4. It is a white solid, stable at room temperature. The following is a description of the nature, use, preparation and safety information of (S)-Lin:

Nature:
(S)-is a photosensitive compound that is soluble in some organic solvents, such as ether, methanol and acetonitrile. Its melting point is about 70-72°C.

Use:
(S)-is a commonly used aminomethyl protecting reagent, which is widely used for the protection of aminomethyl in organic synthesis. It can react with aminomethyl to form a protected ketal of aminomethyl morpholine, preventing it from accidentally reacting during the reaction. In pharmaceutical synthesis and organic synthesis, the protection of the amino methyl group is often necessary, so (S)-phenyl has important application value in this regard.

Preparation Method:
(S)-can be prepared by the reaction of the organic compound Boc-aminomethyl and morpholine. The reaction is typically conducted under an inert atmosphere to minimize contact of the reactants with air and prevent photosensitizer activity.

Safety Information:
The safety information about (S)-is rarely reported, but general chemical laboratory safety regulations should be followed during operation. Wear appropriate personal protective equipment such as lab clothes, glasses, and gloves. Prevent inhalation, ingestion or skin contact, avoid severe vibration or strong impact. When using this compound, waste should be disposed of properly and local waste disposal regulations should be followed. Before performing any operation, it is best to read the safety data sheet of the compound and follow the safe operation recommendations provided.

Last Update：2024-04-09 21:54:55