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CAS

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255876-30-3

C74H91O18SiN3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 255876-30-3 Structure

  • Basic information

    1. Product Name: C74H91O18SiN3
    2. Synonyms: C74H91O18SiN3
    3. CAS NO:255876-30-3
    4. Molecular Formula:
    5. Molecular Weight: 1338.63
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 255876-30-3.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: C74H91O18SiN3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C74H91O18SiN3(255876-30-3)
    11. EPA Substance Registry System: C74H91O18SiN3(255876-30-3)

  • 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: 255876-30-3(Hazardous Substances Data)

255876-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 255876-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,5,8,7 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 255876-30:
(8*2)+(7*5)+(6*5)+(5*8)+(4*7)+(3*6)+(2*3)+(1*0)=173
173 % 10 = 3
So 255876-30-3 is a valid CAS Registry Number.

255876-30-3Upstream product

255876-30-3Downstream Products

255876-30-3Relevant articles and documents

Syntheses of GM4 and GM3 Intermediates via Alkylation and Subsequent Intramolecular Glycosidation of 2-Alkoxy-2-phenylthioacetate

Takahashi, Takashi,Tsukamoto, Hirokazu,Yamada, Haruo

, p. 1885 - 1887 (1999)

(Matrix presented) We developed a new method for α-glycoside formation of sialyl conjugates based on alkylation and subsequent intramolecular glycosidation of 2-alkoxy-2-phenylthioacetate. By this method we succeeded in the syntheses of GM4 and

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