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CAS

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77679-23-3

N1-benzyl-2-phosphonoacetamidine hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 77679-23-3 Structure

  • Basic information

    1. Product Name: N1-benzyl-2-phosphonoacetamidine hydrochloride
    2. Synonyms:
    3. CAS NO:77679-23-3
    4. Molecular Formula:
    5. Molecular Weight: 264.649
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 77679-23-3.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: N1-benzyl-2-phosphonoacetamidine hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: N1-benzyl-2-phosphonoacetamidine hydrochloride(77679-23-3)
    11. EPA Substance Registry System: N1-benzyl-2-phosphonoacetamidine hydrochloride(77679-23-3)

  • 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: 77679-23-3(Hazardous Substances Data)

77679-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77679-23-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,7 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77679-23:
(7*7)+(6*7)+(5*6)+(4*7)+(3*9)+(2*2)+(1*3)=183
183 % 10 = 3
So 77679-23-3 is a valid CAS Registry Number.

77679-23-3Downstream Products

77679-23-3Relevant articles and documents

Inhibitors of Pyrimidine Biosynthesis. Part 2. The Synthesis of Amidine Phosphonates as Potential Inhibitors of Carbamoyl Phosphate Synthase

Wharton, Clifford J.,Wrigglesworth, Roger

, p. 433 - 436 (1981)

The synthesis of a series of amidine phosphonates (8) and (9) via a thioimidate intermediate is described.

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