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193953-63-8

C26H41N2O7PSi is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 193953-63-8 Structure

  • Basic information

    1. Product Name: C26H41N2O7PSi
    2. Synonyms:
    3. CAS NO:193953-63-8
    4. Molecular Formula:
    5. Molecular Weight: 552.68
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 193953-63-8.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: C26H41N2O7PSi(CAS DataBase Reference)
    10. NIST Chemistry Reference: C26H41N2O7PSi(193953-63-8)
    11. EPA Substance Registry System: C26H41N2O7PSi(193953-63-8)

  • 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: 193953-63-8(Hazardous Substances Data)

193953-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193953-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,9,5 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 193953-63:
(8*1)+(7*9)+(6*3)+(5*9)+(4*5)+(3*3)+(2*6)+(1*3)=178
178 % 10 = 8
So 193953-63-8 is a valid CAS Registry Number.

193953-63-8Relevant articles and documents

Oligosaccharide synthesis based on glycosyl donors and accepters carrying phosphorus-containing leaving groups

Hashimoto, Shun-Ichi,Sakamoto, Hiroki,Honda, Takeshi,Ikegami, Shiro

, p. 5181 - 5184 (1997)

Efficient synthetic strategy for oligosaccharides has been developed by exploiting the difference in anomeric reactivity between glycosyl donors and acceptors carrying phosphorus-containing leaving groups, wherein, the tetramethylphosphoroamidate group plays a pivotal role as anomeric protective group as well as leaving group.

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