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453524-99-7

2,3,4,6-tetra-O-benzoyl-5-deoxy-5-thio-α-D-glucopyranosyl trichloroacetimidate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 453524-99-7 Structure

  • Basic information

    1. Product Name: 2,3,4,6-tetra-O-benzoyl-5-deoxy-5-thio-α-D-glucopyranosyl trichloroacetimidate
    2. Synonyms: 2,3,4,6-tetra-O-benzoyl-5-deoxy-5-thio-α-D-glucopyranosyl trichloroacetimidate
    3. CAS NO:453524-99-7
    4. Molecular Formula:
    5. Molecular Weight: 757.045
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 453524-99-7.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: 2,3,4,6-tetra-O-benzoyl-5-deoxy-5-thio-α-D-glucopyranosyl trichloroacetimidate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4,6-tetra-O-benzoyl-5-deoxy-5-thio-α-D-glucopyranosyl trichloroacetimidate(453524-99-7)
    11. EPA Substance Registry System: 2,3,4,6-tetra-O-benzoyl-5-deoxy-5-thio-α-D-glucopyranosyl trichloroacetimidate(453524-99-7)

  • 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: 453524-99-7(Hazardous Substances Data)

453524-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 453524-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,3,5,2 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 453524-99:
(8*4)+(7*5)+(6*3)+(5*5)+(4*2)+(3*4)+(2*9)+(1*9)=157
157 % 10 = 7
So 453524-99-7 is a valid CAS Registry Number.

453524-99-7Relevant articles and documents

Synthetic studies on oligosaccharides composed of 5-thioglucopyranose units

Morii, Yasuharu,Matsuda, Hiroko,Ohara, Keiichiro,Hashimoto, Masaru,Miyairi, Kazuo,Okuno, Toshikatsu

, p. 5113 - 5144 (2007/10/03)

Glycosylation reactions of 5-thioglucopyranosyl trichloroacetimidates bearing ethereal protective groups at the 2-O-position 14-15, and 37 proceed smoothly to give α-glycosides stereoselectively by using a catalytic amount of silyl triflate. This methodol

β-selective glycosylation of 5-thioglucopyranose derivatives; syntheses of β-(1 → 6) linked 5′-thioglucopyranosyl disaccharides

Ohara, Keiichiro,Matsuda, Hiroko,Hashimoto, Masaru,Miyairi, Kazuo,Okuno, Toshikatsu

, p. 626 - 627 (2007/10/03)

β-Stereoselctive and effective glycosylation with 5-thioglucopyranose was achieved by performing the reaction with pivaloyl- or benzoyl-protected glucopyranosyl trichloroacetimidates and BF3OEt2, a glycosyl activator, when C6-OH gluc

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