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511544-63-1

dimethyl (Ss,1S,2R)-(-)-1-chloro-2-(4-nitrophenyl)-2-(p-toluenesulfinamido)ethylphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 511544-63-1 Structure

  • Basic information

    1. Product Name: dimethyl (Ss,1S,2R)-(-)-1-chloro-2-(4-nitrophenyl)-2-(p-toluenesulfinamido)ethylphosphonate
    2. Synonyms: dimethyl (Ss,1S,2R)-(-)-1-chloro-2-(4-nitrophenyl)-2-(p-toluenesulfinamido)ethylphosphonate
    3. CAS NO:511544-63-1
    4. Molecular Formula:
    5. Molecular Weight: 446.848
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 511544-63-1.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: dimethyl (Ss,1S,2R)-(-)-1-chloro-2-(4-nitrophenyl)-2-(p-toluenesulfinamido)ethylphosphonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl (Ss,1S,2R)-(-)-1-chloro-2-(4-nitrophenyl)-2-(p-toluenesulfinamido)ethylphosphonate(511544-63-1)
    11. EPA Substance Registry System: dimethyl (Ss,1S,2R)-(-)-1-chloro-2-(4-nitrophenyl)-2-(p-toluenesulfinamido)ethylphosphonate(511544-63-1)

  • 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: 511544-63-1(Hazardous Substances Data)

511544-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 511544-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,1,5,4 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 511544-63:
(8*5)+(7*1)+(6*1)+(5*5)+(4*4)+(3*4)+(2*6)+(1*3)=121
121 % 10 = 1
So 511544-63-1 is a valid CAS Registry Number.

511544-63-1Downstream Products

511544-63-1Relevant articles and documents

Asymmetric synthesis of aziridine 2-phosphonates from enantiopure sulfinimines (N-sulfinyl imines). Synthesis of α-amino phosphonates

Davis, Franklin A.,Wu, Yongzhong,Yan, Hongxing,McCoull, William,Prasad, Kavirayani R.

, p. 2410 - 2419 (2003)

An aza-Darzens reaction, involving the addition of chloromethylphosphonate anions to enantiopure sulfinimines, has been developed for the asymmetric synthesis of aziridine 2-phosphonates. Best results involve cyclization of the syn and anti diastereomeric

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