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C33H31N3O8 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104557-10-0 Structure
  • Basic information

    1. Product Name: C33H31N3O8
    2. Synonyms: C33H31N3O8
    3. CAS NO:104557-10-0
    4. Molecular Formula:
    5. Molecular Weight: 597.624
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104557-10-0.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: C33H31N3O8(CAS DataBase Reference)
    10. NIST Chemistry Reference: C33H31N3O8(104557-10-0)
    11. EPA Substance Registry System: C33H31N3O8(104557-10-0)
  • 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: 104557-10-0(Hazardous Substances Data)

104557-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104557-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,5 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104557-10:
(8*1)+(7*0)+(6*4)+(5*5)+(4*5)+(3*7)+(2*1)+(1*0)=100
100 % 10 = 0
So 104557-10-0 is a valid CAS Registry Number.

104557-10-0Downstream Products

104557-10-0Relevant articles and documents

REGIOSELECTIVE PROTECTION OF CARBOHYDRATE DERIVATIVES. PART. 20. SIMPLE, EFFICIENT 2'-O-DEACYLATION OF FULLY ACYLATED PURINE AND PYRIMIDINE RIBONUCLEOSIDES THROUGH tert-BUTOXIDE

Nishino, Shigeyoshi,Takamura, Hatsuko,Ishido, Yoshiharu

, p. 1995 - 2004 (2007/10/02)

A simple treatment of fully aroylated purine and pyrimidine ribonucleosides with pulverized potassium tert-butoxide in tetrahydrofuran (THF) or dichloromethane under a controlled condition gave a mixture of the corresponding di-O-aroyl derivatives in which 2'-OH derivatives are preponderant over 3'-OH derivatives; 3',5'-di-O-benzoyluridine, N4,3',5'-tribenzoylcytidine, N4,3',5'-tri-O-toluoylcytidine, N2,3',5'-tribenzoylguanosine, and N2,isobutyryl-3',5'-di-O-benzoylguanosine were obtained crystalline in 80 percent, 78 percent, 72 percent, 67 percent, and 65 percent yields, respectively.

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