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CAS

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607721-06-2

6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 607721-06-2 Structure

  • Basic information

    1. Product Name: 6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate
    2. Synonyms: 6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate
    3. CAS NO:607721-06-2
    4. Molecular Formula:
    5. Molecular Weight: 678.907
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 607721-06-2.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: 6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate(607721-06-2)
    11. EPA Substance Registry System: 6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate(607721-06-2)

  • 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: 607721-06-2(Hazardous Substances Data)

607721-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 607721-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,7,2 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 607721-06:
(8*6)+(7*0)+(6*7)+(5*7)+(4*2)+(3*1)+(2*0)+(1*6)=142
142 % 10 = 2
So 607721-06-2 is a valid CAS Registry Number.

607721-06-2Relevant articles and documents

Synthesis of the blocked pentasaccharide derivative related to the repeating unit of the O-antigen from Shigella dysenteriae type 3 in the form of its allyl glycoside

Sarkar, Sujit Kumar,Roy, Nirmolendu

, p. 285 - 296 (2003)

Starting from D-galactosamine hydrochloride, D-galactose and D-glucose, the tetrasaccharide derivative allyl 2,3,6-tri-O-benzyl-4-O-[methyl (R)-2-propanoate]-β-D-glucopyranosyl-(1→6)-2,3, 4-tri-O-benzyl-α-D-glucopyranosyl-(1→4)-2,6-di-O-benzyl-3-O-(3,4, 6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl) -α-D-galactopyranoside has been synthesized via block synthesis strategy, with one of the blocks containing a methyl (R)-2-propanoate group. Manipulation of protecting groups of this tetrasaccharide derivative followed by its reaction with a galactofuranoside donor afforded the desired pentasaccharide derivative in the form of its allyl glycoside related to the reapeating unit of Shigella dysenteriae type 3.

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