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5'-O-(4,4'-dimethoxytrityl)-N6-dimethylaminomethyleneadenosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 73793-98-3 Structure
  • Basic information

    1. Product Name: 5'-O-(4,4'-dimethoxytrityl)-N6-dimethylaminomethyleneadenosine
    2. Synonyms: 5'-O-(4,4'-dimethoxytrityl)-N6-dimethylaminomethyleneadenosine
    3. CAS NO:73793-98-3
    4. Molecular Formula:
    5. Molecular Weight: 624.696
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73793-98-3.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: 5'-O-(4,4'-dimethoxytrityl)-N6-dimethylaminomethyleneadenosine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5'-O-(4,4'-dimethoxytrityl)-N6-dimethylaminomethyleneadenosine(73793-98-3)
    11. EPA Substance Registry System: 5'-O-(4,4'-dimethoxytrityl)-N6-dimethylaminomethyleneadenosine(73793-98-3)
  • 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: 73793-98-3(Hazardous Substances Data)

73793-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73793-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,9 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73793-98:
(7*7)+(6*3)+(5*7)+(4*9)+(3*3)+(2*9)+(1*8)=173
173 % 10 = 3
So 73793-98-3 is a valid CAS Registry Number.

73793-98-3Relevant articles and documents

High yield protection of purine ribonucleosides for H-phosphonate RNA synthesis

Zhang, Xiaohu,Abad, Jose-Luis,Huang, Qingtao,Zeng, Fan,Gaffney, Barbara L.,Jones, Roger A.

, p. 7135 - 7138 (1997)

We report a new method for protecting nucleosides for hydrogen phosphonate RNA synthesis that gives very high yields for the purines. This method is based on our finding that, for adenosine and guanosine, silylation of a mixture of 2' and 3'H-phosphonates in the presence of DBU is highly selective for the 2' hydroxyl.

Synthesis of 9-β-D-(Xylofuranosyl)adenine from Adenosine

Xi, Cheng,Jun-Dong, Zhang,Li-He, Zhang

, p. 383 - 384 (2007/10/02)

Protected adenosine 3 was oxidized using Moffatt reagent to give the 3'-ketoadenosine 4 in 60percent yield.Stereospecific reduction of 4 with sodium borohydride in the presence of triethylamine at -18 deg C followed by deprotection effects the inversion o

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