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1359704-84-9

Tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate is a spirocyclic chemical compound with the molecular formula C12H19NO3. It features a tert-butyl group, an oxo group, and a carboxylate group, making it a versatile building block in organic synthesis and medicinal chemistry for the creation of pharmaceuticals and bioactive compounds. Its distinctive structure and functional groups contribute to its value as an intermediate for preparing complex molecules and as a research tool in biological processes and drug discovery.

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  • 1359704-84-9 Structure

  • Basic information

    1. Product Name: tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate
    2. Synonyms: tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate
    3. CAS NO:1359704-84-9
    4. Molecular Formula: C13H21NO3
    5. Molecular Weight: 239.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1359704-84-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 348.6±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.12±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -0.78±0.20(Predicted)
    10. CAS DataBase Reference: tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate(1359704-84-9)
    12. EPA Substance Registry System: tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate(1359704-84-9)

  • 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: 1359704-84-9(Hazardous Substances Data)

1359704-84-9 Usage

Uses

Used in Organic Synthesis:
Tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate is used as a building block for the synthesis of various pharmaceuticals and bioactive compounds due to its unique spirocyclic structure and functional groups, which facilitate the preparation of complex molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate is utilized as a key intermediate in the development of new drugs, leveraging its structural and functional attributes to enhance the properties and efficacy of pharmaceutical agents.
Used in Research and Drug Discovery:
Tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate serves as a research tool in studying biological processes and aiding in drug discovery, providing insights into molecular interactions and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1359704-84-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,9,7,0 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1359704-84:
(9*1)+(8*3)+(7*5)+(6*9)+(5*7)+(4*0)+(3*4)+(2*8)+(1*4)=189
189 % 10 = 9
So 1359704-84-9 is a valid CAS Registry Number.

1359704-84-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate

1.2 Other means of identification

Product number -
Other names 6-BOC-2-OXO-6-AZASPIRO[3.5]NONANE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1359704-84-9 SDS

1359704-84-9Relevant articles and documents

Stereoselective Diboration of Spirocyclobutenes: A Platform for the Synthesis of Spirocycles with Orthogonal Exit Vectors

Nóvoa, Luis,Trulli, Laura,Parra, Alejandro,Tortosa, Mariola

, p. 11763 - 11768 (2021/04/26)

The diastereo- and enantioselective diboration of spirocyclobutenes provides a platform for the rapid preparation of a wide variety of chiral spirocyclic building blocks. The chemoselective functionalization of the carbon-boron bond in the products, including a stereospecific sp3-sp2 Suzuki–Miyaura cross-coupling reaction, provides a powerful tool to control the directionality and the nature of the exit vectors in the spirocyclic framework.

PYRAZOLE COMPOUNDS AS BTK INHIBITORS

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Paragraph 26; 27, (2015/09/23)

The present invention encompasses compounds of the formula (I) wherein the groups R1, Cy, and Y are defined herein, which are suitable for the treatment of diseases related to BTK, process of making, pharmaceutical preparations which contain compounds and their methods of use.

SPIROCYCLIC MOLECULES AS PROTEIN KINASE INHIBITORS

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Paragraph 00256-00258, (2013/03/26)

The present invention relates to spirocyclic compounds of formula I, namely spirocyclic (1H-pyrazol-4-yl)-3-(1-(2,6-dichloro-3-fiuorophenyl) ethoxy)pyridin-2-amines having protein kinase inhibitory activity, and methods of synthesizing and using such compounds. Preferred compounds are c-Met and/or ALK inhibitors useful for the treatment of abnormal cell growth, such as cancers

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