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116556-64-0

Methyl 2-acetamido-3,4-di-O-benzyl-2-deoxy-6-O-tosyl-α-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 116556-64-0 Structure

  • Basic information

    1. Product Name: Methyl 2-acetamido-3,4-di-O-benzyl-2-deoxy-6-O-tosyl-α-D-glucopyranoside
    2. Synonyms: Methyl 2-acetamido-3,4-di-O-benzyl-2-deoxy-6-O-tosyl-α-D-glucopyranoside
    3. CAS NO:116556-64-0
    4. Molecular Formula:
    5. Molecular Weight: 569.676
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116556-64-0.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 2-acetamido-3,4-di-O-benzyl-2-deoxy-6-O-tosyl-α-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 2-acetamido-3,4-di-O-benzyl-2-deoxy-6-O-tosyl-α-D-glucopyranoside(116556-64-0)
    11. EPA Substance Registry System: Methyl 2-acetamido-3,4-di-O-benzyl-2-deoxy-6-O-tosyl-α-D-glucopyranoside(116556-64-0)

  • 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: 116556-64-0(Hazardous Substances Data)

116556-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116556-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,5 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116556-64:
(8*1)+(7*1)+(6*6)+(5*5)+(4*5)+(3*6)+(2*6)+(1*4)=130
130 % 10 = 0
So 116556-64-0 is a valid CAS Registry Number.

116556-64-0Relevant articles and documents

Design and synthesis of N–acetylglucosamine derived 5a-carbasugar analogues as glycosidase inhibitors

Narayana, Chintam,Kumari, Priti,Ide, Daisuke,Hoshino, Nasako,Kato, Atsushi,Sagar, Ram

, p. 1957 - 1964 (2018)

An efficient synthesis of new six-membered carbasugars in both L-form and D-form starting from N–acetylglucosamine is described. The key synthetic steps involved regioselective protection and deprotection, Ferrier carbocyclization, Peterson olefination, h

Synthesis of Methyl Glycosides of D-Quinovosamine and D-Fucosamine

Roy, Abhijit,Ray, Asim K.,Mukherjee, Atryee,Roy, Nirmolendu

, p. 1165 - 1167 (2007/10/02)

Methyl glycosides of D-quinovosamine (7) has been synthesized from D-glucosamine hydrochloride in eight steps.Starting from N-acetyl-D-galactosamine, methyl glycoside of D-fucosamine has been synthesized in six steps.LAH reduction of 6-O-tosyl derivative

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