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3',5'-O-1,1,3,3-tetraisopropyldisiloxyl-2'-O-methyl-3-N-(2-nitrobenzene)sulfenyluridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 98889-57-7 Structure
  • Basic information

    1. Product Name: 3',5'-O-1,1,3,3-tetraisopropyldisiloxyl-2'-O-methyl-3-N-(2-nitrobenzene)sulfenyluridine
    2. Synonyms: 3',5'-O-1,1,3,3-tetraisopropyldisiloxyl-2'-O-methyl-3-N-(2-nitrobenzene)sulfenyluridine
    3. CAS NO:98889-57-7
    4. Molecular Formula:
    5. Molecular Weight: 653.901
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 98889-57-7.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: 3',5'-O-1,1,3,3-tetraisopropyldisiloxyl-2'-O-methyl-3-N-(2-nitrobenzene)sulfenyluridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3',5'-O-1,1,3,3-tetraisopropyldisiloxyl-2'-O-methyl-3-N-(2-nitrobenzene)sulfenyluridine(98889-57-7)
    11. EPA Substance Registry System: 3',5'-O-1,1,3,3-tetraisopropyldisiloxyl-2'-O-methyl-3-N-(2-nitrobenzene)sulfenyluridine(98889-57-7)
  • 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: 98889-57-7(Hazardous Substances Data)

98889-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98889-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,8,8 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98889-57:
(7*9)+(6*8)+(5*8)+(4*8)+(3*9)+(2*5)+(1*7)=227
227 % 10 = 7
So 98889-57-7 is a valid CAS Registry Number.

98889-57-7Relevant articles and documents

Synthesis of C-5 and N-3 Arenesulfenyl Uridines. Preparation and Properties of a New Class of Uracil Protecting Group

Welch, C. J.,Bazin, H.,Heikkila, J.,Chattopadhyaya, J.

, p. 203 - 212 (2007/10/02)

The nature and position of the ring substituent of an arenesulfenyl chloride control the regiospecific formation of either a C-5 substituted product, as in compounds 3a-3d, or a N-3 substituted product, as in compound 2a-2c.Arenesulfenyl groups have been subsequently found to successfully protect the urethane function of the residue as exemplified by teh synthesis of 2'-O-methyl uridine and oligoribonucleotide building blocks.

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