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130222-85-4

5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130222-85-4 Structure

  • Basic information

    1. Product Name: 5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol
    2. Synonyms: 5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol
    3. CAS NO:130222-85-4
    4. Molecular Formula:
    5. Molecular Weight: 430.616
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130222-85-4.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-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol(130222-85-4)
    11. EPA Substance Registry System: 5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol(130222-85-4)

  • 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: 130222-85-4(Hazardous Substances Data)

130222-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130222-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,2 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130222-85:
(8*1)+(7*3)+(6*0)+(5*2)+(4*2)+(3*2)+(2*8)+(1*5)=74
74 % 10 = 4
So 130222-85-4 is a valid CAS Registry Number.

130222-85-4Relevant articles and documents

Stereoselective synthesis of selenium-containing glycoconjugates via the mitsunobu reaction

Cermola, Flavio,De Nisco, Mauro,Manfra, Michele,Pedatella, Silvana,Serpico, Luigia

, (2021)

A simple and efficient route for the synthesis of new glycoconjugates has been developed. The approach acts as a model for a mini-library of compounds with a deoxy-selenosugar core joined to a polyphenolic moiety with well-known antioxidant properties. An unexpected stereocontrol detected in the Mitsunobu key reaction led to the most attractive product showing a natural Dconfiguration. Thus, we were able to obtain the target molecules from the commercially available D-ribose via a shorter and convenient sequence of reactions.

Method For Rapidly Evaluating Performance Of Short Interfering RNA With Novel Chemical Modifications

-

, (2012/10/08)

It is an object of the instant invention to provide a method for the rapid evaluation of novel sugar modifications to be used in siRNA synthesis including the rapid evaluation of chemical modification patterns within the siRNA to effectuate increased stability and ultimately increased efficacy of a siRNA therapeutic. It is a further object of the instant invention to provide novel nucleosides useful for siRNA therapy.

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