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1029432-35-6

(S)-tert-Butyl 1-(2-aminophenyl)pyrrolidin-3-ylcarbamate is a chiral chemical compound with the molecular formula C15H23N3O2. It is a pyrrolidine derivative featuring a tert-butyl group, an aminophenyl group, and a carbamate group attached to the pyrrolidine ring. (S)-tert-Butyl 1-(2-aminophenyl)pyrrolidin-3-ylcarbamate's chirality indicates the presence of a non-superimposable mirror image, or enantiomer. Its chemical structure suggests potential biological activity, making it a candidate for pharmaceutical applications or as a building block in the synthesis of other compounds. Further research is necessary to explore its properties and possible uses.

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  • 1029432-35-6 Structure

  • Basic information

    1. Product Name: (S)-tert-Butyl 1-(2-aminophenyl)pyrrolidin-3-ylcarbamate
    2. Synonyms: (S)-tert-Butyl 1-(2-aminophenyl)pyrrolidin-3-ylcarbamate
    3. CAS NO:1029432-35-6
    4. Molecular Formula: C15H23N3O2
    5. Molecular Weight: 277.36202
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1029432-35-6.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-tert-Butyl 1-(2-aminophenyl)pyrrolidin-3-ylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-tert-Butyl 1-(2-aminophenyl)pyrrolidin-3-ylcarbamate(1029432-35-6)
    11. EPA Substance Registry System: (S)-tert-Butyl 1-(2-aminophenyl)pyrrolidin-3-ylcarbamate(1029432-35-6)

  • 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: 1029432-35-6(Hazardous Substances Data)

1029432-35-6 Usage

Uses

Used in Pharmaceutical Industry:
(S)-tert-Butyl 1-(2-aminophenyl)pyrrolidin-3-ylcarbamate is used as a potential pharmaceutical agent due to its unique chemical structure and chirality. The presence of various functional groups in the molecule may allow it to interact with biological targets, making it a candidate for the development of new drugs.
Used in Chemical Synthesis:
(S)-tert-Butyl 1-(2-aminophenyl)pyrrolidin-3-ylcarbamate can be used as a building block in the synthesis of other complex organic compounds. Its versatile structure, including the aminophenyl and carbamate groups, may facilitate the creation of novel molecules with specific properties and applications in various fields, including materials science, agrochemistry, and the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 1029432-35-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,9,4,3 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1029432-35:
(9*1)+(8*0)+(7*2)+(6*9)+(5*4)+(4*3)+(3*2)+(2*3)+(1*5)=126
126 % 10 = 6
So 1029432-35-6 is a valid CAS Registry Number.

1029432-35-6Downstream Products

1029432-35-6Relevant articles and documents

Kinase inhibitor, and preparation and application of kinase inhibitor

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Paragraph 0302-0304; 0307; 0308, (2018/09/11)

The invention provides a compound shown as a formula (I), or a stereoisomer, a tautomer, nitrogen oxide, metabolite, a prodrug, pharmaceutically acceptable salt or solvate of the compound, and application of the compound to preparing drugs or drug compositions for treating Pim kinase-mediated diseases.

ANILINOPIPERAZINE DERIVATIVES AND METHODS OF USE THEREOF

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Page/Page column 184-185, (2008/12/05)

The present invention relates to novel Anilinopiperazine Derivatives of Formula (I), compositions comprising the Anilinopiperazine Derivatives, and methods for using the Anilinopiperazine Derivatives for treating or preventing a proliferative disorder, cancer, an anti-proliferative disorder, inflammation, arthritis, a central nervous system disorder, a cardiovascular disease, alopecia, a neuronal disease, an ischemic injury, a viral disease, a fungal infection, or a disorder related to the activity of a protein kinase.

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