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CAS

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1448617-52-4

2-naphthyl 3,4-di-O-benzyl-2,6-dideoxy-β-L-arabinohexopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1448617-52-4 Structure

  • Basic information

    1. Product Name: 2-naphthyl 3,4-di-O-benzyl-2,6-dideoxy-β-L-arabinohexopyranoside
    2. Synonyms: 2-naphthyl 3,4-di-O-benzyl-2,6-dideoxy-β-L-arabinohexopyranoside
    3. CAS NO:1448617-52-4
    4. Molecular Formula:
    5. Molecular Weight: 454.566
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1448617-52-4.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: 2-naphthyl 3,4-di-O-benzyl-2,6-dideoxy-β-L-arabinohexopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-naphthyl 3,4-di-O-benzyl-2,6-dideoxy-β-L-arabinohexopyranoside(1448617-52-4)
    11. EPA Substance Registry System: 2-naphthyl 3,4-di-O-benzyl-2,6-dideoxy-β-L-arabinohexopyranoside(1448617-52-4)

  • 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: 1448617-52-4(Hazardous Substances Data)

1448617-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1448617-52-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,6,1 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1448617-52:
(9*1)+(8*4)+(7*4)+(6*8)+(5*6)+(4*1)+(3*7)+(2*5)+(1*2)=184
184 % 10 = 4
So 1448617-52-4 is a valid CAS Registry Number.

1448617-52-4Upstream product

1448617-52-4Downstream Products

1448617-52-4Relevant articles and documents

Reagent controlled β-specific dehydrative glycosylation reactions with 2-deoxy-sugars

Issa, John Paul,Lloyd, Dina,Steliotes, Emily,Bennett, Clay S.

, p. 4170 - 4173 (2013)

N-Sulfonyl imidazoles activate 2-deoxy-sugar hemiacetals for glycosylation presumably by converting them into glycosyl sulfonates in situ. By matching the leaving group ability of the sulfonate with the reactivity of the donor, it is possible to obtain β-

Reagent-Controlled Stereoselective Glycosylation

-

Paragraph 0217; 0218; 0219; 0220; 0221; 0222; 0223, (2015/02/19)

Provided are methods for the efficient stereoselective formation of glycosidic bonds, without recourse to prosthetic or directing groups.

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