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146578-30-5

Methyl 2-O-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 146578-30-5 Structure

  • Basic information

    1. Product Name: Methyl 2-O-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside
    2. Synonyms: Methyl 2-O-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside
    3. CAS NO:146578-30-5
    4. Molecular Formula:
    5. Molecular Weight: 330.402
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146578-30-5.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-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 2-O-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside(146578-30-5)
    11. EPA Substance Registry System: Methyl 2-O-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside(146578-30-5)

  • 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: 146578-30-5(Hazardous Substances Data)

146578-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146578-30-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,5,7 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 146578-30:
(8*1)+(7*4)+(6*6)+(5*5)+(4*7)+(3*8)+(2*3)+(1*0)=155
155 % 10 = 5
So 146578-30-5 is a valid CAS Registry Number.

146578-30-5Relevant articles and documents

Synthesis of a tetrasaccharide donor corresponding to the O-specific polysaccharide of Shigella dysenteriae type 1

Pozsgay,Glaudemans,Robbins,Schneerson

, p. 259 - 273 (2007/10/02)

O-(2,4-Di-O-benzoyl-3-O-chloroacetyl-α-L-rhamnopyranosyl)-(1 → 2)-O-(3,4,6-tri-O-benzoyl-α-D-galactopyranosyl)-(1 → 3)-O-(2-acetamido-4,6-di-O-acetyl-2-deoxy-α-D-glucopyranosyl)-(1 → 3)-2,4-di-O-benzoyl-α-L-rhamnopyranosyl trichloroacetimidate (1) was syn

Synthesis of tetrasaccharide building block of the O-specific polysaccharide of Shigella dysenteriae type 1

Pozsgay,Glaudemans,Robbins,Schneerson

, p. 10249 - 10264 (2007/10/02)

A glycosyl trichloroacetimidate derivative (1) of the tetrasaccharide α-D-Galp-(1→3)-α-D-GlcpNAc-(1→3)-α-L-Rhap-(1→3)-α-L-Rhap was synthesized in a highly stereoselective, stepwise manner, using methyl 1-thioglycosides of L-rhamnose, 2-azido-2-deoxy-D-glucose and D-galactose, as major intermediates. The protecting group scenario in compound 1 permits regioselective deblocking at its 'non-reducing end' unit. Therefore 1 is a suitable intermediate for the preparation of extended fragments of the title polysaccharide.

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