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(S)-2-AminoMethyl-1-Boc-azetidine is a chemical compound widely utilized in scientific research and pharmaceutical applications. It features an azetidine core, a four-membered cyclic amine, which is essential for the synthesis of bioactive molecules. The Boc (tert-butoxycarbonyl) group in the compound provides protection for the amine functionality during the synthesis of more complex molecules. The S-isomer designation of this chemical highlights its specific spatial configuration, a factor that can markedly affect its biological activity in medicinal chemistry. It is synthesized through laboratory procedures and should be handled with care due to potential hazards.

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  • 1007873-90-6 Structure
  • Basic information

    1. Product Name: (S)-2-AMinoMethyl-1-Boc-azetidine
    2. Synonyms: (S)-2-AMinoMethyl-1-Boc-azetidine;(S)-2-AMinoMethyl-1-Boc-a...;(S)-tert-Butyl 2-(aMinoMethyl)azetidine-1-carboxylate;tert-butyl (2S)-2-(aminomethyl)azetidine-1-carboxylate;(2S)-1-Boc-2-azetidinemethanamine
    3. CAS NO:1007873-90-6
    4. Molecular Formula: C9H18N2O2
    5. Molecular Weight: 186.25142
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1007873-90-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-2-AMinoMethyl-1-Boc-azetidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-AMinoMethyl-1-Boc-azetidine(1007873-90-6)
    11. EPA Substance Registry System: (S)-2-AMinoMethyl-1-Boc-azetidine(1007873-90-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1007873-90-6(Hazardous Substances Data)

1007873-90-6 Usage

Uses

Used in Pharmaceutical Industry:
(S)-2-AminoMethyl-1-Boc-azetidine is used as a key intermediate in the synthesis of various pharmaceutical compounds for its ability to contribute to the formation of bioactive molecules. The presence of the azetidine core and the Boc group allows for the creation of complex molecular structures with potential therapeutic applications.
Used in Scientific Research:
In the field of scientific research, (S)-2-AminoMethyl-1-Boc-azetidine serves as a valuable compound for studying the effects of spatial configuration on biological activity. Its S-isomer designation makes it an ideal candidate for exploring the relationship between molecular structure and pharmacological properties.
Used in Organic Synthesis:
(S)-2-AminoMethyl-1-Boc-azetidine is utilized as a building block in organic synthesis for the creation of a variety of organic compounds. Its unique structure and functional groups enable the development of new chemical entities with potential applications in various industries.
Used in Drug Development:
In drug development, (S)-2-AminoMethyl-1-Boc-azetidine is employed as a precursor in the synthesis of new drug candidates. Its specific spatial configuration and the presence of the Boc group make it a versatile component in the design and synthesis of molecules with potential therapeutic effects.
Used in Chemical Education:
(S)-2-AminoMethyl-1-Boc-azetidine can also be used in chemical education to demonstrate the principles of stereochemistry and the importance of spatial configuration in the biological activity of molecules. It provides a practical example for teaching the synthesis and manipulation of complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1007873-90-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,8,7 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1007873-90:
(9*1)+(8*0)+(7*0)+(6*7)+(5*8)+(4*7)+(3*3)+(2*9)+(1*0)=146
146 % 10 = 6
So 1007873-90-6 is a valid CAS Registry Number.

1007873-90-6Downstream Products

1007873-90-6Relevant articles and documents

AZETIDINE COMPOUNDS AS OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 24, (2010/09/07)

The invention relates to novel azetidine compounds of formula (I), wherein R1, R2, and X are as described in the description and their use as orexin receptor antagonists.

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