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Methyl 2-O-allyl-4,6-di-O-benzyl-α-[*]-mannopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Methyl 2-O-allyl-4,6-di-O-benzyl-α-[*]-mannopyranoside

    Cas No: 219313-07-2

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  • 219313-07-2 Structure
  • Basic information

    1. Product Name: Methyl 2-O-allyl-4,6-di-O-benzyl-α-[*]-mannopyranoside
    2. Synonyms: Methyl 2-O-allyl-4,6-di-O-benzyl-α-[*]-mannopyranoside
    3. CAS NO:219313-07-2
    4. Molecular Formula:
    5. Molecular Weight: 414.499
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 219313-07-2.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 2-O-allyl-4,6-di-O-benzyl-α-[*]-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 2-O-allyl-4,6-di-O-benzyl-α-[*]-mannopyranoside(219313-07-2)
    11. EPA Substance Registry System: Methyl 2-O-allyl-4,6-di-O-benzyl-α-[*]-mannopyranoside(219313-07-2)
  • 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: 219313-07-2(Hazardous Substances Data)

219313-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219313-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,3,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 219313-07:
(8*2)+(7*1)+(6*9)+(5*3)+(4*1)+(3*3)+(2*0)+(1*7)=112
112 % 10 = 2
So 219313-07-2 is a valid CAS Registry Number.

219313-07-2Relevant articles and documents

Synthesis and glycosidic coupling reaction of substituted 2,6-dioxabicyco[3.1.1] heptanes: 1,3-anhydro-2-azido-4,6-di-O-benzyl-2-deoxy-β-D-mannopyranose

Yang, Guangbin,Kong, Fanzuo

, p. 77 - 83 (2007/10/03)

The title 1,3-anhydro sugar was synthesized from methyl α-D-glucopyranoside. The key intermediate for the synthesis was 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranosyl chloride (11) which was transformed into the target compound by ring closure with potassium tert-butoxide. Copyright (C) 1998 Elsevier Science Ltd.

SYNTHESIS OF A DI-AND A TRI-SACCHARIDE RELATED TO THE K-ANTIGEN OF Klebsiella TYPE 10 AND A STUDY OF THEIR INHIBITION IN THE PRECIPITIN REACTION

Sarkar, Arun K.,Ray, Asim K.,Roy, Nirmolendu

, p. 181 - 190 (2007/10/02)

Synthesis of methyl 3-O-α--galactopyranosyl-α--mannopyranoside (10) and methyl 3-O-α--galactopyranosyl-2-O-(β--glucopyranosyluronic acid)-α--mannopyranoside (11) in good yield are described.Both 10 and 11 significantly inhibit antigen-antib

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