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2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane is a synthetic spiro-compound characterized by its unique molecular structure and reactivity. The "Boc" in its name signifies the presence of a tert-butyloxycarbonyl protective group, while the digits denote the arrangement and type of atoms within the compound. As a non-naturally occurring compound, it is synthesized in controlled scientific environments for research and experimental purposes, with potential applications in pharmaceuticals and synthetic organic chemistry.

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  • 1105664-04-7 Structure
  • Basic information

    1. Product Name: 2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane
    2. Synonyms: 2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane;2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane - B7177
    3. CAS NO:1105664-04-7
    4. Molecular Formula: C12H18N2O4
    5. Molecular Weight: 254.28232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1105664-04-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 465.2±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.26±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 12.51±0.20(Predicted)
    10. CAS DataBase Reference: 2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane(1105664-04-7)
    12. EPA Substance Registry System: 2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane(1105664-04-7)
  • 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: 1105664-04-7(Hazardous Substances Data)

1105664-04-7 Usage

Uses

Used in Pharmaceutical Industry:
2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane is used as a chemical intermediate for the synthesis of various pharmaceutical compounds due to its unique structure and reactivity. Its potential applications in drug development are currently under investigation.
Used in Synthetic Organic Chemistry:
In the field of synthetic organic chemistry, 2-Boc-7,9-dioxo-2,6-diazaspiro[3.5]nonane serves as a key building block for the creation of complex organic molecules. Its unique structure allows for versatile reactions and transformations, making it a valuable component in the synthesis of novel organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1105664-04-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,5,6,6 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1105664-04:
(9*1)+(8*1)+(7*0)+(6*5)+(5*6)+(4*6)+(3*4)+(2*0)+(1*4)=117
117 % 10 = 7
So 1105664-04-7 is a valid CAS Registry Number.

1105664-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 5,7-dioxo-2,8-diazaspiro[3.5]nonane-2-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 7,9-dioxo-2,6-diazaspiro[3.5]nonane-2-carboxylate

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:1105664-04-7 SDS

1105664-04-7Upstream product

1105664-04-7Downstream Products

1105664-04-7Relevant articles and documents

In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part II

Revesz, Laszlo,Schlapbach, Achim,Aichholz, Reiner,Dawson, Janet,Feifel, Roland,Hawtin, Stuart,Littlewood-Evans, Amanda,Koch, Guido,Kroemer, Markus,Moebitz, Henrik,Scheufler, Clemens,Velcicky, Juraj,Huppertz, Christine

scheme or table, p. 4719 - 4723 (2010/09/16)

Spirocyclopropane- and spiroazetidine-substituted tetracycles 13D-E and 16A are described as orally active MK2 inhibitors. The spiroazetidine derivatives are potent MK2 inhibitors with IC50 50

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