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C62H57N4O17P*C6H15N is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131853-67-3 Structure
  • Basic information

    1. Product Name: C62H57N4O17P*C6H15N
    2. Synonyms:
    3. CAS NO:131853-67-3
    4. Molecular Formula:
    5. Molecular Weight: 1262.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131853-67-3.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: C62H57N4O17P*C6H15N(CAS DataBase Reference)
    10. NIST Chemistry Reference: C62H57N4O17P*C6H15N(131853-67-3)
    11. EPA Substance Registry System: C62H57N4O17P*C6H15N(131853-67-3)
  • 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: 131853-67-3(Hazardous Substances Data)

131853-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131853-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,8,5 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 131853-67:
(8*1)+(7*3)+(6*1)+(5*8)+(4*5)+(3*3)+(2*6)+(1*7)=123
123 % 10 = 3
So 131853-67-3 is a valid CAS Registry Number.

131853-67-3Downstream Products

131853-67-3Relevant articles and documents

Nucleoside 3'-N,N-dialkylphosphonamidates: Novel building blocks for oligonucleotide synthesis

Wada,Ishikawa,Hata

, p. 6363 - 6366 (2007/10/02)

Nucleoside 3'-N,N-diisopropylphosphonamidates reacted with tris(2,4,6-tribromophenoxy)dichlorophosphorane (BDCP) to generate the corresponding aminophosphorochloridites without cleavage of the P-N bond. The reaction was applied to internucleotidic bond formation.

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