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CAS

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1369423-47-1

diphenyl 4-fluorobenzyl phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1369423-47-1 Structure

  • Basic information

    1. Product Name: diphenyl 4-fluorobenzyl phosphate
    2. Synonyms: diphenyl 4-fluorobenzyl phosphate
    3. CAS NO:1369423-47-1
    4. Molecular Formula:
    5. Molecular Weight: 358.306
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1369423-47-1.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: diphenyl 4-fluorobenzyl phosphate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diphenyl 4-fluorobenzyl phosphate(1369423-47-1)
    11. EPA Substance Registry System: diphenyl 4-fluorobenzyl phosphate(1369423-47-1)

  • 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: 1369423-47-1(Hazardous Substances Data)

1369423-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1369423-47-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,4,2 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1369423-47:
(9*1)+(8*3)+(7*6)+(6*9)+(5*4)+(4*2)+(3*3)+(2*4)+(1*7)=181
181 % 10 = 1
So 1369423-47-1 is a valid CAS Registry Number.

1369423-47-1Relevant articles and documents

Benzylic phosphates as electrophiles in the palladium-catalyzed asymmetric benzylation of azlactones

Trost, Barry M.,Czabaniuk, Lara C.

, p. 5778 - 5781 (2012/05/07)

Palladium-catalyzed asymmetric benzylation has been demonstrated with azlactones as prochiral nucleophiles in the presence of chiral bisphosphine ligands. Benzylic electrophiles are utilized under two sets of reaction conditions to construct a new tetrasubstituted stereocenter. Electron density of the phenyl ring dictates the reaction conditions, including the leaving group. The reported methodology represents a novel asymmetric carbon-carbon bond formation in an amino acid precursor.

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