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methyl-(O5-benzyl-O2,O3-carbonyl-α-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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  • 69603-05-0 Structure
  • Basic information

    1. Product Name: methyl-(O5-benzyl-O2,O3-carbonyl-α-D-ribofuranoside)
    2. Synonyms:
    3. CAS NO:69603-05-0
    4. Molecular Formula:
    5. Molecular Weight: 280.277
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69603-05-0.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-(O5-benzyl-O2,O3-carbonyl-α-D-ribofuranoside)(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl-(O5-benzyl-O2,O3-carbonyl-α-D-ribofuranoside)(69603-05-0)
    11. EPA Substance Registry System: methyl-(O5-benzyl-O2,O3-carbonyl-α-D-ribofuranoside)(69603-05-0)
  • 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: 69603-05-0(Hazardous Substances Data)

69603-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69603-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,0 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69603-05:
(7*6)+(6*9)+(5*6)+(4*0)+(3*3)+(2*0)+(1*5)=140
140 % 10 = 0
So 69603-05-0 is a valid CAS Registry Number.

69603-05-0Downstream Products

69603-05-0Relevant articles and documents

Synthesis of methyl 2-O-allyl-(and 3-O-allyl-)5-O-benzyl-β-D-ribofuranoside

Desai,Gigg,Gigg

, p. 209 - 221 (2007/10/03)

D-Ribose was converted into methyl 5-O-benzyl-β-D-ribofuranoside and this, on tin-mediated allylation, gave a mixture of the 2-O-allyl and 3-O-allyl derivatives which were separated by chromatography. The more polar isomer was characterised as the 3-O-allyl derivative after conversion via 3-O-allyl-5-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranose (which was also synthesised from 3-O-allyl-1,2:5,6-di-O-isopropylidene-α-D-allofuranose) into the known 5-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranose. Methyl 3-O-allyl-5-O-benzyl-β-D-ribofuranoside was converted into methyl 2-O-allyl-5-O-benzyl-β-D-ribofuranoside via methyl 2-O-allyl-5-O-benzyl-3-O(prop-1-enyl)-β-D-ribofuranoside.

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