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ethyl 1-<(1,3S,4-tribenzyloxy-2R-butoxy)methyl>-1,2,4-triazole-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 117486-37-0 Structure
  • Basic information

    1. Product Name: ethyl 1-<(1,3S,4-tribenzyloxy-2R-butoxy)methyl>-1,2,4-triazole-3-carboxylate
    2. Synonyms: ethyl 1-<(1,3S,4-tribenzyloxy-2R-butoxy)methyl>-1,2,4-triazole-3-carboxylate
    3. CAS NO:117486-37-0
    4. Molecular Formula:
    5. Molecular Weight: 545.635
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 117486-37-0.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: ethyl 1-<(1,3S,4-tribenzyloxy-2R-butoxy)methyl>-1,2,4-triazole-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 1-<(1,3S,4-tribenzyloxy-2R-butoxy)methyl>-1,2,4-triazole-3-carboxylate(117486-37-0)
    11. EPA Substance Registry System: ethyl 1-<(1,3S,4-tribenzyloxy-2R-butoxy)methyl>-1,2,4-triazole-3-carboxylate(117486-37-0)
  • 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: 117486-37-0(Hazardous Substances Data)

117486-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117486-37-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,4,8 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117486-37:
(8*1)+(7*1)+(6*7)+(5*4)+(4*8)+(3*6)+(2*3)+(1*7)=140
140 % 10 = 0
So 117486-37-0 is a valid CAS Registry Number.

117486-37-0Relevant articles and documents

A practical synthesis of ethyl 1,2,4-triazole-3-carboxylate and its use in the formation of chiral 1',2'-seco-nucleosides of ribavirin

Vemishetti,Leiby,Abushanab,Panzica

, p. 651 - 654 (2007/10/02)

A practical and efficient synthesis of ethyl 1,2,4-triazole-3-carboxylate (6a, R'' = H) from ethyl carboethoxyformimidate hydrochloride is described. Alkylation of this heterocycle with the chloromethyl ethers of 1,3-O-dibenzylbutane-1,2R,3S-triol and 1,3

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