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2-Azabicyclo[2.1.1]hexane-2-carboxylicacid,ethylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 217093-76-0 Structure
  • Basic information

    1. Product Name: 2-Azabicyclo[2.1.1]hexane-2-carboxylicacid,ethylester(9CI)
    2. Synonyms: 2-Azabicyclo[2.1.1]hexane-2-carboxylicacid,ethylester(9CI)
    3. CAS NO:217093-76-0
    4. Molecular Formula: C8H13NO2
    5. Molecular Weight: 155.19
    6. EINECS: N/A
    7. Product Categories: CARBOXYLICESTER
    8. Mol File: 217093-76-0.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: 2-Azabicyclo[2.1.1]hexane-2-carboxylicacid,ethylester(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Azabicyclo[2.1.1]hexane-2-carboxylicacid,ethylester(9CI)(217093-76-0)
    11. EPA Substance Registry System: 2-Azabicyclo[2.1.1]hexane-2-carboxylicacid,ethylester(9CI)(217093-76-0)
  • 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: 217093-76-0(Hazardous Substances Data)

217093-76-0 Usage

Structure

Bicyclic compound with a nitrogen atom in the bridging ring

Use in Organic Synthesis

Building block for the synthesis of pharmaceutical drugs and biologically active molecules

Applications in Medicinal Chemistry

Utilized for drug synthesis

Chiral Auxiliary in Asymmetric Synthesis

Assists in creating optically pure compounds

Ligand in Catalysis

Enhances chemical reactions in catalytic processes

Potential Applications

Pharmaceutical industry
Agrochemical industry
Material industry

Check Digit Verification of cas no

The CAS Registry Mumber 217093-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,0,9 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 217093-76:
(8*2)+(7*1)+(6*7)+(5*0)+(4*9)+(3*3)+(2*7)+(1*6)=130
130 % 10 = 0
So 217093-76-0 is a valid CAS Registry Number.

217093-76-0SDS

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 ethyl 3-azabicyclo[2.1.1]hexane-3-carboxylate

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:217093-76-0 SDS

217093-76-0Relevant articles and documents

HETROARYL BENZAMIDE DERIVATIVES FOR USE AS GLK ACTIVATORS IN THE TREATMENT OF DIABETES

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Page/Page column 185, (2008/06/13)

Compounds of Formula (I) wherein: R1 is hydroxymethyl; R2 is selected from -C(O)NR4R5, SO2NR4R5, S(O)pR4 and HET-2; HET-1 is a 5- or 6-membered, optionally substituted C-linked heteroaryl ring; HET-2 is a 4-, 5- or 6-membered, C- or N-linked optionally substituted heterocyclyl ring; R3 is selected from halo, fluoromethyl, difluoromethyl, trifluoromethyl, methyl, methoxy and cyano; R4 is selected from for example hydrogen, optionally substituted (1-4C)alkyl and HET-2; R5 is hydrogen or (1-4C)alkyl; or R4 and R5 together with the nitrogen atom to which they are attached may form a heterocyclyl ring system as defined by HET-3; HET-3 is for example an optionally substituted N-linked, 4, 5 or 6 membered, saturated or partially unsaturated heterocyclyl ring; p is (independently at each occurrence) 0, 1 or 2; m is 0 or 1; n is 0, 1 or 2; provided that when m is 0, then n is 1 or 2; or a salt, pro drug or solvate thereof, are described. Their use as GLK activators, pharmaceutical compositions containing them, and processes for their preparation are also described.

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