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78038-31-0

Methyl 5-O-benzyl-α,β-D-ribofuranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78038-31-0 Structure

  • Basic information

    1. Product Name: Methyl 5-O-benzyl-α,β-D-ribofuranoside
    2. Synonyms: Methyl 5-O-benzyl-α,β-D-ribofuranoside
    3. CAS NO:78038-31-0
    4. Molecular Formula:
    5. Molecular Weight: 254.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78038-31-0.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: Methyl 5-O-benzyl-α,β-D-ribofuranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 5-O-benzyl-α,β-D-ribofuranoside(78038-31-0)
    11. EPA Substance Registry System: Methyl 5-O-benzyl-α,β-D-ribofuranoside(78038-31-0)

  • 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: 78038-31-0(Hazardous Substances Data)

78038-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78038-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,3 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 78038-31:
(7*7)+(6*8)+(5*0)+(4*3)+(3*8)+(2*3)+(1*1)=140
140 % 10 = 0
So 78038-31-0 is a valid CAS Registry Number.

78038-31-0Relevant articles and documents

Synthesis and biological evaluation of novel isonucleosides with 1,2,4-triazole-3-carboxamide

Kim, Myong Jung,Chung, Soon Yong,Chun, Moon Woo

, p. 2653 - 2663 (2007/10/03)

Novel 1,2,4-triazole isonucleosides (1 and 2) were efficiently synthesized starting from D-ribose and D-xylose, respectively. The key steps were condensation of cyclic sulfate 8 with methyl-1,2,4-triazole-3-carboxylate and nucleophilic displacement of the

SYNTHESIS OF FOUR STEREOISOMERS OF 4-AMINO-2-(HYDROXY-METHYL)TETRAHYDROFURAN-4-CARBOXYLIC ACID

Yoshimura, Juji,Kondo, Shiro,Ihara, Masaki,Hashimoto, Hironobu

, p. 129 - 142 (2007/10/02)

The 5-benzyl ether, 15, of a 1,2,,4,5-pentanetetrol of known 2S configuration was made by a multistep synthesis from D-ribose.Ring-closure of the 1-O-otosyl derivative, 17, with retention of configuration, followed by oxidation, gave the 2S enantiomer, 22

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