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CAS

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1237503-02-4

6,6-dichloro-3-[(1S)-1-phenylethylamino]-1-methyl-3-phosphabicyclo[3.1.0]hexane 3-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1237503-02-4 Structure

  • Basic information

    1. Product Name: 6,6-dichloro-3-[(1S)-1-phenylethylamino]-1-methyl-3-phosphabicyclo[3.1.0]hexane 3-oxide
    2. Synonyms:
    3. CAS NO:1237503-02-4
    4. Molecular Formula:
    5. Molecular Weight: 318.183
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1237503-02-4.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: 6,6-dichloro-3-[(1S)-1-phenylethylamino]-1-methyl-3-phosphabicyclo[3.1.0]hexane 3-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,6-dichloro-3-[(1S)-1-phenylethylamino]-1-methyl-3-phosphabicyclo[3.1.0]hexane 3-oxide(1237503-02-4)
    11. EPA Substance Registry System: 6,6-dichloro-3-[(1S)-1-phenylethylamino]-1-methyl-3-phosphabicyclo[3.1.0]hexane 3-oxide(1237503-02-4)

  • 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: 1237503-02-4(Hazardous Substances Data)

1237503-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1237503-02-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,7,5,0 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1237503-02:
(9*1)+(8*2)+(7*3)+(6*7)+(5*5)+(4*0)+(3*3)+(2*0)+(1*2)=124
124 % 10 = 4
So 1237503-02-4 is a valid CAS Registry Number.

1237503-02-4Downstream Products

1237503-02-4Relevant articles and documents

The synthesis of optically active P-heterocycles

Keglevich, Gyoergy,Dvorszki, Judit,Ujj, Viktoria,Ludanyi, Krisztina

, p. 271 - 277 (2011/07/09)

Optically active 1-alkoxy- and 1-amino- 3-phospholene oxides were synthesized by the reaction of the corresponding 1-chloro-3-phospholene oxides with (1 R,2S,5R)-(-)menthol and (S)-(-)-α- phenylethylamine. The 3-methyl-3-phospholene oxides were subjected to dichlorocyclopropanation under liquid-liquid phase transfer catalytic conditions to afford the 3-phosphabicyclo[3.1.0]hexane 3-oxides as a mixture of four diastereomers. Thermolysis of the menthyl-phosphabicyclohexane oxides led to the corresponding 1 2-dihydrophosphinine oxide as a diastereomeric mixture of two double-bond isomers. As a result of additional steps, the dichlorocarbene addition reaction of the 1-menthyl- 3,4-dimethyl-3-phospholene oxide resulted in eventually, the formation of a 4-dichloromethylene-1,4-dihydrophosphinine oxide.

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