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172405-48-0

9H-Purine-9-acetic acid, 1,6-dihydro-2-[[(4-methoxyphenyl)diphenylmethyl]amino]-6-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 172405-48-0 Structure

  • Basic information

    1. Product Name: 9H-Purine-9-acetic acid, 1,6-dihydro-2-[[(4-methoxyphenyl)diphenylmethyl]amino]-6-oxo-
    2. Synonyms:
    3. CAS NO:172405-48-0
    4. Molecular Formula: C27H23N5O4
    5. Molecular Weight: 481.511
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 172405-48-0.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: 9H-Purine-9-acetic acid, 1,6-dihydro-2-[[(4-methoxyphenyl)diphenylmethyl]amino]-6-oxo-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9H-Purine-9-acetic acid, 1,6-dihydro-2-[[(4-methoxyphenyl)diphenylmethyl]amino]-6-oxo-(172405-48-0)
    11. EPA Substance Registry System: 9H-Purine-9-acetic acid, 1,6-dihydro-2-[[(4-methoxyphenyl)diphenylmethyl]amino]-6-oxo-(172405-48-0)

  • 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: 172405-48-0(Hazardous Substances Data)

172405-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172405-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,4,0 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 172405-48:
(8*1)+(7*7)+(6*2)+(5*4)+(4*0)+(3*5)+(2*4)+(1*8)=120
120 % 10 = 0
So 172405-48-0 is a valid CAS Registry Number.

172405-48-0Relevant articles and documents

Dde-protected PNA monomers, orthogonal to Fmoc, for the synthesis of PNA-peptide conjugates

Bialy, Laurent,Díaz-Mochón, Juan José,Specker, Edgar,Keinicke, Lise,Bradley, Mark

, p. 8295 - 8305 (2007/10/03)

Peptide nucleic acids have become, arguably, one of the most interesting of DNA mimics. Herein the efficient solution phase synthesis of four novel 1-(4,4-dimethyl-2,6-dioxacyclohexylidene)ethyl/4-methoxytrityl (Dde/Mmt) protected PNA monomers is reported

Synthesis of polyamide nucleic acids (PNAs) using a novel Fmoc/Mmt protecting-group combination

Breipohl,Knolle,Langner,O'Malley,Uhlmann

, p. 665 - 670 (2007/10/03)

The preparation of 9-Fluorenylmethoxycarbonyl(Fmoc) protected building blocks for the synthesis of polyamide nucleic acids (PNAs) is described. Use of 4-Methoxyphenyldiphenylmethyl (Mmt)-protecting groups for the exocyclic amino function of the nucleobase

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