N-Boc-aMinoMethylaMidine Hydrochloride

N-Boc-aMinoMethylaMidine Hydrochloride - Names and Identifiers

Name	Tert-butyl amidinomethylcarbamate hydrochloride
Synonyms	N-Boc-aMinoMethylaMidine Hydrochloride Tert-butyl amidinomethylcarbamate hydrochloride n-(2-amino-2-iminoethyl)carbamic acid tert-butyl ester TERT-BUTYL N-(CARBAMIMIDOYLMETHYL)CARBAMATE HYDROCHLORIDE tert-butyl N-(2-amino-2-iminoethyl)carbamate,hydrochloride N-(2-AMino-2-iMinoethyl)carbaMic Acid 1,1-DiMethylethyl Ester N-(2-Amino-2-iminoethyl)carbamic acid tert-butyl ester hydrochloride (2-Amino-2-iminoethyl)carbamic acid tert-butyl ester monohydrochloride
CAS	691898-38-1

N-Boc-aMinoMethylaMidine Hydrochloride - Physico-chemical Properties

Molecular Formula	C7H15N3O2.HCl
Molar Mass	210
Melting Point	>160°C (dec.)
Solubility	DMSO (Slightly), Methanol (Slightly), Water (Slightly)
Appearance	Solid
Color	White to Off-White
Storage Condition	Inert atmosphere,Room Temperature

N-Boc-aMinoMethylaMidine Hydrochloride - Introduction

Tert-butyl amidinomethylcarbamate hydrochloride, chemical name for Tert-butyl amidinomethylcarbamate hydrochloride, is an organic compound.

Nature:
The Tert-butyl amidinomethylcarbamate hydrochloride is a white crystalline powder with certain stability and is relatively stable at room temperature. It is soluble in many organic solvents, such as methanol, ethanol, etc., but has low solubility in water.

Use:
Tert-butyl amidinomethylcarbamate hydrochloride are widely used in organic synthesis. It is often used as a protecting group in organic synthesis to protect the amino group and prevent other reactions. In addition, it can also be used as an intermediate, in the synthesis of drugs and other organic compounds play a key role.

Preparation Method:
The preparation of Tert-butyl amidinomethylcarbamate hydrochloride is usually carried out by the following steps:
1. First, N-BOC-ethylenediamine was synthesized. Ethylenediamine is reacted with tert-butoxycarbonyl (BOC) anhydride to give N-BOC-ethylenediamine.
2. N-BOC-ethylenediamine is then reacted with chloroformyl chloride to obtain N-BOC-aminoethylamidine hydrochloride.

Safety Information:
Tert-butyl the safety of amidinomethylcarbamate hydrochloride is high, it is still necessary to follow general laboratory safety practices. It may be irritating to the skin, eyes and respiratory tract, so it is necessary to wear appropriate protective measures, such as laboratory gloves, glasses and masks. During storage, avoid contact with air and moisture and keep it dry.

Last Update：2024-04-09 21:01:54