
Benzyl ((1S,3S)-3-(methylamino)cyclobutyl)carbamate hydrochloride
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Category:Pharmaceutical Materials Own Brand:MT /MOQ:100KG /From China/ B2B only.
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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