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155351-71-6

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  • 155351-71-6 Structure

  • Basic information

    1. Product Name: 2-(benzyloxy)-3-methoxy-5-<5-(methoxymethoxy)ethyl>benzaldehyde trimethylene acetal
    2. Synonyms: 2-(benzyloxy)-3-methoxy-5-<5-(methoxymethoxy)ethyl>benzaldehyde trimethylene acetal
    3. CAS NO:155351-71-6
    4. Molecular Formula:
    5. Molecular Weight: 388.461
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 155351-71-6.mol
    9. Article Data: 1

  • 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: 2-(benzyloxy)-3-methoxy-5-<5-(methoxymethoxy)ethyl>benzaldehyde trimethylene acetal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(benzyloxy)-3-methoxy-5-<5-(methoxymethoxy)ethyl>benzaldehyde trimethylene acetal(155351-71-6)
    11. EPA Substance Registry System: 2-(benzyloxy)-3-methoxy-5-<5-(methoxymethoxy)ethyl>benzaldehyde trimethylene acetal(155351-71-6)

  • 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: 155351-71-6(Hazardous Substances Data)

155351-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155351-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,3,5 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155351-71:
(8*1)+(7*5)+(6*5)+(5*3)+(4*5)+(3*1)+(2*7)+(1*1)=126
126 % 10 = 6
So 155351-71-6 is a valid CAS Registry Number.

155351-71-6Relevant articles and documents

Total synthesis of the gilvocarcins

Hosoya, Takamitsu,Takashiro, Eiji,Matsumoto, Takashi,Suzuki, Keisuke

, p. 1004 - 1015 (2007/10/02)

Convergent total syntheses of the aryl C-glycoside antibiotics gilvocarcin M (1a) and gilvocarcin V (1b) have been accomplished. Key steps include (1) contrasteric coupling of D-fucofuranosyl acetate 27 with iodophenol 26, which was achieved by employing

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