Benzyl ((1S,3S)-3-(methylamino)cyclobutyl)carbamate hydrochloride

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Category:Pharmaceutical Materials   Own Brand:MT  /MOQ:100KG  /From China/  B2B only.

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Introduction

(1S, 3S) -3- (methylamino) cyclobutyl) aminoformate benzyl ester hydrochloride is a compound, and its properties, uses, preparation methods, and safety information are as follows:

Nature:

-Appearance: May be in solid or liquid form.

-Having benzyl ester functional group and hydrochloride salt functional group.

-Having chiral centers, described as 1S, 3S isomers.

Purpose:

-Further understanding of its research background is needed for specific purposes.

Manufacturing method:

-The preparation method may involve the reaction synthesis of benzyl carbamate, cyclobutane, and hydrochloric acid.

Name Carbamic acid, N-[cis-3-(methylamino)cyclobutyl]-, phenylmethyl ester, hydrochloride (1:1)
Synonyms Benzyl (cis-3-(methylamino)cyclobutyl)carbamate hydrochloride
CAS 2204290-99-1

Fundamental Chemical Properties

Property Specification
Chemical Name Benzyl ((1S,3S)-3-(methylamino)cyclobutyl)carbamate hydrochloride
CAS Number 2204290-99-1
Molecular Formula C₁₄H₂₁ClN₂O₂
Molecular Weight 284.78 g/mol
Appearance White to off-white crystalline powder
Melting Point 180-185°C (dec.)
Solubility Soluble in water, methanol, DMSO

Key Functional Properties & Applications

Function Application
Pharmaceutical intermediate API synthesis
Chiral building block Asymmetric synthesis
Amine protecting group Peptide chemistry
Cyclobutane derivative Medicinal chemistry research
Carbamate reagent Organic transformations

Safety & Handling Information

Parameter Guidelines
Skin contact Use protective gloves
Eye contact Rinse immediately with water
Storage 2-8°C under inert atmosphere
Stability Sensitive to moisture and heat
Disposal Dispose as hazardous chemical waste

This stereochemically defined cyclobutyl derivative serves as a valuable chiral intermediate in pharmaceutical research, particularly for the development of novel therapeutic agents. The hydrochloride salt form enhances its stability and handling properties.

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