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683209-01-0

Phosphonic acid, [[4-[(1R)-1-azido-3-butenyl]phenyl]methyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 683209-01-0 Structure

  • Basic information

    1. Product Name: Phosphonic acid, [[4-[(1R)-1-azido-3-butenyl]phenyl]methyl]-, diethyl ester
    2. Synonyms:
    3. CAS NO:683209-01-0
    4. Molecular Formula: C15H22N3O3P
    5. Molecular Weight: 323.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 683209-01-0.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: Phosphonic acid, [[4-[(1R)-1-azido-3-butenyl]phenyl]methyl]-, diethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphonic acid, [[4-[(1R)-1-azido-3-butenyl]phenyl]methyl]-, diethyl ester(683209-01-0)
    11. EPA Substance Registry System: Phosphonic acid, [[4-[(1R)-1-azido-3-butenyl]phenyl]methyl]-, diethyl ester(683209-01-0)

  • 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: 683209-01-0(Hazardous Substances Data)

683209-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 683209-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,3,2,0 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 683209-01:
(8*6)+(7*8)+(6*3)+(5*2)+(4*0)+(3*9)+(2*0)+(1*1)=160
160 % 10 = 0
So 683209-01-0 is a valid CAS Registry Number.

683209-01-0Relevant articles and documents

Enantioselective Synthesis of Metathesis-Derived Ureapeptoid Macrocycles

Wang, Xiang-Zhu,Burke Jr., Terrence R.

, p. 469 - 472 (2007/10/03)

Ring-closing metathesis (RCM) was used for the preparation of the first member of a new class of ureapeptoid-containing macrocycles. Key to the approach was the enantioselective synthesis of functionalized carbamoyl alkenylglycine equivalents using (-)-B-allyldiisopinocampheylborane [(-)-d-Ipc2Ball]-mediated asymmetric allylation.

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