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CAS

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125736-09-6

9-tert-butyl 2-methyl 2-(phenylselanyl)-9-azabicyclo[4.2.1]nonane-2,9-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125736-09-6 Structure

  • Basic information

    1. Product Name: 9-tert-butyl 2-methyl 2-(phenylselanyl)-9-azabicyclo[4.2.1]nonane-2,9-dicarboxylate
    2. Synonyms:
    3. CAS NO:125736-09-6
    4. Molecular Formula: C21H29NO4Se
    5. Molecular Weight: 438.4193
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125736-09-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 494.6°C at 760 mmHg
    3. Flash Point: 252.9°C
    4. Appearance: N/A
    5. Density: N/A
    6. Vapor Pressure: 6.37E-10mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 9-tert-butyl 2-methyl 2-(phenylselanyl)-9-azabicyclo[4.2.1]nonane-2,9-dicarboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 9-tert-butyl 2-methyl 2-(phenylselanyl)-9-azabicyclo[4.2.1]nonane-2,9-dicarboxylate(125736-09-6)
    12. EPA Substance Registry System: 9-tert-butyl 2-methyl 2-(phenylselanyl)-9-azabicyclo[4.2.1]nonane-2,9-dicarboxylate(125736-09-6)

  • 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: 125736-09-6(Hazardous Substances Data)

125736-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125736-09-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,7,3 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 125736-09:
(8*1)+(7*2)+(6*5)+(5*7)+(4*3)+(3*6)+(2*0)+(1*9)=126
126 % 10 = 6
So 125736-09-6 is a valid CAS Registry Number.

125736-09-6Relevant articles and documents

Chirospecific Syntheses of Nitrogen and Side-Chain Modified Anatoxin Analogues. Synthesis of (1R)-Anatoxinal and (1R)-Anatoxinic Acid Derivatives

Howard, Michael H.,Sardina, F. Javier,Rapoport, Henry

, p. 2829 - 2838 (2007/10/02)

A straightforward and good yielding route to side-chain analogues of the potent neurotoxin and neurotransmitter (+)-anatoxin (1) has been developed.Peroxy acid oxidation of the (silyloxy)butadiene 43 derived from readily synthesized, optically pure (1R)-t-BOC-anatoxin (42) affords silyloxy ketone 44.Fluorolysis of 44 followed by oxidative cleavage of the resultant α-hydroxy ketone 45 gives a mixture of α,β-unsaturated acid 46 and ester 41 in 57percent combined yield.Other approaches to these compounds, based on literature precedent, failed. (1R)-t-BOC-anatoxinic acid (46) then serves as educt for the synthesis of a wide variety of anatoxin derivatives with modified side-chain functionality.These analogues, designed to serve as probes of the antagonist binding site of the nicotinic acetylcholine receptor, include alcohol, aldehyde, amide, hydroxamate, and oxime ether functional groups.

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