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5-formyl-1-(2'-deoxy-3'-5'-di-O-p-toluoyl-β-D-erythro-pentofuranosyl)-6-azauracil is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97776-66-4 Structure
  • Basic information

    1. Product Name: 5-formyl-1-(2'-deoxy-3'-5'-di-O-p-toluoyl-β-D-erythro-pentofuranosyl)-6-azauracil
    2. Synonyms: 5-formyl-1-(2'-deoxy-3'-5'-di-O-p-toluoyl-β-D-erythro-pentofuranosyl)-6-azauracil
    3. CAS NO:97776-66-4
    4. Molecular Formula:
    5. Molecular Weight: 493.473
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97776-66-4.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-formyl-1-(2'-deoxy-3'-5'-di-O-p-toluoyl-β-D-erythro-pentofuranosyl)-6-azauracil(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-formyl-1-(2'-deoxy-3'-5'-di-O-p-toluoyl-β-D-erythro-pentofuranosyl)-6-azauracil(97776-66-4)
    11. EPA Substance Registry System: 5-formyl-1-(2'-deoxy-3'-5'-di-O-p-toluoyl-β-D-erythro-pentofuranosyl)-6-azauracil(97776-66-4)
  • 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: 97776-66-4(Hazardous Substances Data)

97776-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97776-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,7,7 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97776-66:
(7*9)+(6*7)+(5*7)+(4*7)+(3*6)+(2*6)+(1*6)=204
204 % 10 = 4
So 97776-66-4 is a valid CAS Registry Number.

97776-66-4Relevant articles and documents

Analysis of an Active Deformylation Mechanism of 5-Formyl-deoxycytidine (fdC) in Stem Cells

Sch?n, Alexander,Kaminska, Ewelina,Schelter, Florian,Ponkkonen, Eveliina,Korytiaková, Eva,Schiffers, Sarah,Carell, Thomas

supporting information, p. 5591 - 5594 (2020/03/04)

The removal of 5-methyl-deoxycytidine (mdC) from promoter elements is associated with reactivation of the silenced corresponding genes. It takes place through an active demethylation process involving the oxidation of mdC to 5-hydroxymethyl-deoxycytidine

Synthesis and Antiviral Properties of 5-(2-Substituted vinyl)-6-aza-2'-deoxyuridines

Mitchell, William L.,Ravenscroft, Paul,Hill, Malcolm L.,Knutsen, Lars J.S.,Judkins, Brian D.,et al.

, p. 809 - 816 (2007/10/02)

The following 5-(2-substituted vinyl)-6-aza-2'-deoxyuridines were synthesized: (E)-5-(2-bromovinyl) (2) (6-aza-BVDU), 5-(2-bromo-2-fluorovinyl) (a mixture E and Z isomers) (3), (E)-5-(2-chlorovinyl) (4), (E)-5- (5), 5-(2,2-dibromoviny

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