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CAS

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1436412-07-5

1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-(2-oxo-propyl)piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1436412-07-5 Structure

  • Basic information

    1. Product Name: 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-(2-oxo-propyl)piperidine
    2. Synonyms: 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-(2-oxo-propyl)piperidine
    3. CAS NO:1436412-07-5
    4. Molecular Formula:
    5. Molecular Weight: 403.519
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1436412-07-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-(2-oxo-propyl)piperidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-(2-oxo-propyl)piperidine(1436412-07-5)
    11. EPA Substance Registry System: 1-benzyloxycarbonyl-6S-(4,4-ethylenedioxybutyl)-4R-methyl-2R-(2-oxo-propyl)piperidine(1436412-07-5)

  • 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: 1436412-07-5(Hazardous Substances Data)

1436412-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1436412-07-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,6,4,1 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1436412-07:
(9*1)+(8*4)+(7*3)+(6*6)+(5*4)+(4*1)+(3*2)+(2*0)+(1*7)=135
135 % 10 = 5
So 1436412-07-5 is a valid CAS Registry Number.

1436412-07-5Downstream Products

1436412-07-5Relevant articles and documents

Total synthesis of (-)-hippodamine by stereocontrolled construction of azaphenalene skeleton based on extended one-pot asymmetric azaelectrocyclization

Fujita, Shintaro,Sakaguchi, Taku,Kobayashi, Toyoharu,Tsuchikawa, Hiroshi,Katsumura, Shigeo

, p. 2758 - 2761 (2013/07/19)

The first asymmetric total synthesis of (-)-hippodamine has been accomplished via the concise construction of its azaphenalene core, which is featured by the 2,4,6-chiral piperidine synthesis based on one-pot asymmetric azaelectrocyclization in the partially activated substituent system and the subsequent intramolecular Mannich reaction.

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