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CAS

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380883-52-3

methyl 3,5-di-O-benzyl-2-O-(4-methylbenzoyl)-β-D-[2-2H1]arabinofuranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 380883-52-3 Structure

  • Basic information

    1. Product Name: methyl 3,5-di-O-benzyl-2-O-(4-methylbenzoyl)-β-D-[2-2H1]arabinofuranoside
    2. Synonyms: methyl 3,5-di-O-benzyl-2-O-(4-methylbenzoyl)-β-D-[2-2H1]arabinofuranoside
    3. CAS NO:380883-52-3
    4. Molecular Formula:
    5. Molecular Weight: 463.535
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 380883-52-3.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: methyl 3,5-di-O-benzyl-2-O-(4-methylbenzoyl)-β-D-[2-2H1]arabinofuranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3,5-di-O-benzyl-2-O-(4-methylbenzoyl)-β-D-[2-2H1]arabinofuranoside(380883-52-3)
    11. EPA Substance Registry System: methyl 3,5-di-O-benzyl-2-O-(4-methylbenzoyl)-β-D-[2-2H1]arabinofuranoside(380883-52-3)

  • 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: 380883-52-3(Hazardous Substances Data)

380883-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 380883-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,8,8 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 380883-52:
(8*3)+(7*8)+(6*0)+(5*8)+(4*8)+(3*3)+(2*5)+(1*2)=173
173 % 10 = 3
So 380883-52-3 is a valid CAS Registry Number.

380883-52-3Relevant articles and documents

Synthesis of [2′-2H1]-Ribonucleosides

Foeldesi, Andras,Kundu, Mrinal K.,Dinya, Zoltan,Chattopadhyaya, Jyoti

, p. 742 - 757 (2007/10/03)

New syntheses of C(2′)-deuterated ribonucleosides have been accomplished starting either from 3,5-di-O-benzyl-1-O-methyl-α,β -D-ribofuranose (1b) or 2,3-O-isopropylidene-D-ribose (14), with >97 atom-% D incorporation in both cases. The former is suited to

Studies on the stereoselective synthesis of deuterated D-ribose derivatives

Kundu, Mrinal K.,Foeldesi, Andras,Chattopadhyaya, Jyoti

, p. 633 - 643 (2007/10/03)

In view of the importance of the site-specific substitution of the H-atom by its stable isotope 2H in a stereoselective/stereospecific manner at the pentose sugar residue, decreasing the spectral overcrowding in various regions of 1D and 2D hom

Synthetic studies to improve the deuterium labelling in nucleosides for facilitating structural studies of large RNAs by high-field NMR spectroscopy

Kundu,Trifonova,Dinya,Foeldesi,Chattopadhyaya

, p. 1333 - 1337 (2007/10/03)

Synthetic studies to prepare ribonucleosides deuterated at C2′ and the application of the developed procedures for the synthesis of 2H5-ribonucleosides from 1,2-O-isopropylidene-3-O-benzyl-ribofuranose-3,4,5,5′ -2H4/

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