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1357291-96-3

N6-(benzyloxymethyl)adenosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1357291-96-3 Structure

  • Basic information

    1. Product Name: N6-(benzyloxymethyl)adenosine
    2. Synonyms:
    3. CAS NO:1357291-96-3
    4. Molecular Formula:
    5. Molecular Weight: 387.395
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1357291-96-3.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: N6-(benzyloxymethyl)adenosine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N6-(benzyloxymethyl)adenosine(1357291-96-3)
    11. EPA Substance Registry System: N6-(benzyloxymethyl)adenosine(1357291-96-3)

  • 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: 1357291-96-3(Hazardous Substances Data)

1357291-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1357291-96-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,2,9 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1357291-96:
(9*1)+(8*3)+(7*5)+(6*7)+(5*2)+(4*9)+(3*1)+(2*9)+(1*6)=183
183 % 10 = 3
So 1357291-96-3 is a valid CAS Registry Number.

1357291-96-3Downstream Products

1357291-96-3Relevant articles and documents

N6-Substituted adenosines. Cytokinin and antitumor activities

Kolyachkina, Svetlana V.,Tararov, Vitali I.,Alexeev, Cyril S.,Krivosheev, Dmitry M.,Romanov, Georgy A.,Stepanova, Evgenia V.,Solomko, Eliso S.,Inshakov, Andrey N.,Mikhailov, Sergey N.

scheme or table, p. 1361 - 1378 (2012/04/04)

A series of N6-adenosine derivatives were synthesized by alkylation of N6-acetyl-2',3',5'-tri-O-acetyladenosine (1) with alkyl halides and alcohols. It was shown that propargyl derivative 2a is a good substrate for copper(I) catalyzed Huisgen [3+2] cycloaddition with azides. This click-reaction can be used for preparation of the libraries of 1,2,3-triazolyl modified adenosines. Biological activities of N6-adenosines were studied in two plant and six human cancer cell assays. The remarkable parallel between cytokinin and cytotoxic activities was found. The most cytokinin active compounds 3c-3e at the same time appeared to be the most potent cytotoxic agents.

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