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"6-tert-butyl 1-methyl 6-azaspiro[2.5]octane-1,6-dicarboxylate" is a complex organic compound with the molecular formula C14H23NO4. It features a spiro ring system, which consists of two fused rings sharing a common atom. In this case, the spiro ring system is composed of a six-membered azaspiro ring and an eight-membered carbocycle. The compound has a tert-butyl group (C4H9) attached to the 6-position of the azaspiro ring, a methyl group (CH3) at the 1-position, and two carboxyl groups (COOH) at the 1 and 6 positions, respectively. This chemical is known for its potential applications in pharmaceuticals and as a chiral ligand in asymmetric catalysis. Its unique structure and properties make it an interesting subject for research in organic chemistry and drug development.

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  • SAGECHEM/ 6-tert-butyl 1-methyl 6-azaspiro[2.5]octane-1,6-dicarboxylate /Manufacturer in China

    Cas No: 871727-04-7

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  • 871727-04-7 Structure
  • Basic information

    1. Product Name: 6-tert-butyl 1-methyl 6-azaspiro[2.5]octane-1,6-dicarboxylate
    2. Synonyms: 6-tert-butyl 1-methyl 6-azaspiro[2.5]octane-1,6-dicarboxylate;6-Azaspiro[2.5]octane-1,6-dicarboxylic acid, 6-(1,1-dimethylethyl) 1-methyl ester
    3. CAS NO:871727-04-7
    4. Molecular Formula: C14H23NO4
    5. Molecular Weight: 269.33672
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 871727-04-7.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: 6-tert-butyl 1-methyl 6-azaspiro[2.5]octane-1,6-dicarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-tert-butyl 1-methyl 6-azaspiro[2.5]octane-1,6-dicarboxylate(871727-04-7)
    11. EPA Substance Registry System: 6-tert-butyl 1-methyl 6-azaspiro[2.5]octane-1,6-dicarboxylate(871727-04-7)
  • 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: 871727-04-7(Hazardous Substances Data)

871727-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 871727-04-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,7,2 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 871727-04:
(8*8)+(7*7)+(6*1)+(5*7)+(4*2)+(3*7)+(2*0)+(1*4)=187
187 % 10 = 7
So 871727-04-7 is a valid CAS Registry Number.

871727-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-O-tert-butyl 2-O-methyl 6-azaspiro[2.5]octane-2,6-dicarboxylate

1.2 Other means of identification

Product number -
Other names -

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:871727-04-7 SDS

871727-04-7Relevant articles and documents

Non-aromatic A-ring replacement in the triaryl bis-sulfone CB2 receptor inhibitors

Gilbert, Eric J.,Zhou, Guowei,Wong, Michael K.C.,Tong, Ling,Shankar, Bandarpalle B.,Huang, Chunli,Kelly, Joseph,Lavey, Brian J.,McCombie, Stuart W.,Chen, Lei,Rizvi, Razia,Dong, Youhao,Shu, Youheng,Kozlowski, Joseph A.,Shih, Neng-Yang,Hipkin, R. William,Gonsiorek, Waldemar,Malikzay, Asra,Lunn, Charles A.,Favreau, Len,Lundell, Daniel J.

scheme or table, p. 608 - 611 (2010/05/02)

The triaryl bis-sulfone 1 was modified by converting the aryl A-ring to a piperidine ring. The piperidine ring was further elaborated to a spirocyclopropyl piperidine moiety. The effect on CB2 binding potency, rat calcium channel affinity, and CYP 2C9 inh

CANNABINOID RECEPTOR LIGANDS

-

Page/Page column 49-50, (2008/06/13)

Compounds of Formula (I) and/or pharmaceutically acceptable salts, solvates or prodrugs thereof, or pharmaceutical compositions containing such compounds exhibit anti-inflammatory and immunomodulatory activity, and can be effective asCB2 receptor ligands in treating cancer and inflammatory, immunomodulatory or respiratory diseases or conditions.

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