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87908-20-1

2-methoxyethyl 2,3,4,6-tetra-O-benzyl-β-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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  • 87908-20-1 Structure

  • Basic information

    1. Product Name: 2-methoxyethyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside
    2. Synonyms: 2-methoxyethyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside
    3. CAS NO:87908-20-1
    4. Molecular Formula:
    5. Molecular Weight: 598.736
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87908-20-1.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-methoxyethyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methoxyethyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(87908-20-1)
    11. EPA Substance Registry System: 2-methoxyethyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(87908-20-1)

  • 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: 87908-20-1(Hazardous Substances Data)

87908-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87908-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,0 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87908-20:
(7*8)+(6*7)+(5*9)+(4*0)+(3*8)+(2*2)+(1*0)=171
171 % 10 = 1
So 87908-20-1 is a valid CAS Registry Number.

87908-20-1Relevant articles and documents

A dehydrative glycosylation protocol mediated by nonafluorobutanesulfonyl fluoride (NfF)

Reddy, D. Prabhakar,Tang, Yu,Yu, Biao

, (2020/12/21)

A new dehydrative glycosylation protocol that proceeds through selective activation of glycosyl hemiacetals with nonafluorobutanesulfonyl fluoride (NfF) has been disclosed. Contrary to the major classical glycosylation reactions that proceed under acidic

Catalytic and Atom-Economic Glycosylation using Glycosyl Formates and Cheap Metal Salts

Hammelev, Christian H.,Pedersen, Christian M.,Yang, Liang

, (2020/05/16)

Benzylated glycosyl formates have been synthesized in one step from the corresponding hemiacetal or orthoester with formic acid as the sole reagent. The glycosyl formates are used as glycosyl donors under catalytic conditions with cheap metal catalysts ba

Vessel Effect in C–F Bond Activation Prompts Revised Mechanism and Reveals an Autocatalytic Glycosylation

Nielsen, Michael M.,Qiao, Yan,Wang, Yingxiong,Pedersen, Christian M.

supporting information, p. 140 - 144 (2020/01/22)

Activation of C–F bonds under acidic conditions results in the formation of hydrogen fluoride as the reaction progresses. In the following communication, the effect of the vessel material on such reactions has been investigated and a significant differenc

A NOVEL PROCEDURE FOR THE PREPARATION OF 1-OH SUGAR DERIVATIVES USING 2-METHOXYETHYL GLYCOSIDES

Morishima, Naohiko,Koto, Shinkiti,Kanemitsu, Kumi,Zen, Shonosuke

, p. 1189 - 1190 (2007/10/02)

Treatment of benzyl-protected 2-methoxyethyl glycopyranosides with titanium tetrachloride followed by hydrolysis provides a new method for the preparation of the corresponding 1-OH sugar derivatives.The present method is shown to be useful for the prepara

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