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Benzoic acid, 2-(1-piperidinylMethyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 209806-11-1 Structure
  • Basic information

    1. Product Name: Benzoic acid, 2-(1-piperidinylMethyl)-, ethyl ester
    2. Synonyms: Benzoic acid, 2-(1-piperidinylMethyl)-, ethyl ester
    3. CAS NO:209806-11-1
    4. Molecular Formula: C15H21NO2
    5. Molecular Weight: 247.33274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 209806-11-1.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: Benzoic acid, 2-(1-piperidinylMethyl)-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 2-(1-piperidinylMethyl)-, ethyl ester(209806-11-1)
    11. EPA Substance Registry System: Benzoic acid, 2-(1-piperidinylMethyl)-, ethyl ester(209806-11-1)
  • 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: 209806-11-1(Hazardous Substances Data)

209806-11-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209806-11-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,8,0 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 209806-11:
(8*2)+(7*0)+(6*9)+(5*8)+(4*0)+(3*6)+(2*1)+(1*1)=131
131 % 10 = 1
So 209806-11-1 is a valid CAS Registry Number.

209806-11-1Relevant articles and documents

Tandem Wolff rearrangement-'α-cyclization of tertiary amines' sequence: Synthesis of some 1H-2-benzopyran derivatives

Leost, Francoise,Chantegrel, Bernard,Deshayes, Christian

, p. 6457 - 6474 (2007/10/03)

The thermolyses of dimethyl 1-diazo-2-oxo(2-(N,N-disubstituted aminomethyl)phenyl)-ethylphosphonates 6a-e of the related ester of 6f afford 1-disubstituted amino-1H-2-benzopyran derivatives 9a-f through a 3-step sequence involving Wolff rearrangement, [1,

Tandem Wolff rearrangement-'tert-amino effect' sequence: Synthesis of 2-oxoindolinium enolate and 1H-2-benzopyrane derivatives

Chantegrel,Deshayes,Faure

, p. 7859 - 7862 (2007/10/02)

The thermal decomposition of dimethyl 1-diazo-2-oxo-(2-N,N-disubstituted aminophenyl)ethylphosphonates 1 gave rise to 2-oxoindolinium enolates 3 resulting from a Wolff rearrangement followed by attack of the nitrogen atom on the intermediate ketene moiety

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