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(6R)-7-phenethyl-1,4-dioxa-7-aza-dispiro[4.0.4.3]tridecan-8-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1225384-06-4 Structure
  • Basic information

    1. Product Name: (6R)-7-phenethyl-1,4-dioxa-7-aza-dispiro[4.0.4.3]tridecan-8-one
    2. Synonyms: (6R)-7-phenethyl-1,4-dioxa-7-aza-dispiro[4.0.4.3]tridecan-8-one
    3. CAS NO:1225384-06-4
    4. Molecular Formula:
    5. Molecular Weight: 301.386
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1225384-06-4.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: (6R)-7-phenethyl-1,4-dioxa-7-aza-dispiro[4.0.4.3]tridecan-8-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (6R)-7-phenethyl-1,4-dioxa-7-aza-dispiro[4.0.4.3]tridecan-8-one(1225384-06-4)
    11. EPA Substance Registry System: (6R)-7-phenethyl-1,4-dioxa-7-aza-dispiro[4.0.4.3]tridecan-8-one(1225384-06-4)
  • 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: 1225384-06-4(Hazardous Substances Data)

1225384-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1225384-06-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,5,3,8 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1225384-06:
(9*1)+(8*2)+(7*2)+(6*5)+(5*3)+(4*8)+(3*4)+(2*0)+(1*6)=134
134 % 10 = 4
So 1225384-06-4 is a valid CAS Registry Number.

1225384-06-4Relevant articles and documents

Stereoselective synthesis of enantiopure analogues of (-)-cephalotaxine

Berhal, Farouk,Perard-Viret, Joelle,Royer, Jacques

experimental part, p. 325 - 332 (2010/06/12)

The asymmetric total synthesis of three analogues of (-)-cephalotaxine with structural modification of the aromatic ring was achieved in 16 steps and acceptable overall yields. The procedure used was quite similar to that reported by our group for the tot

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