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358738-57-5

3,5-bis(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-1,2,4-thiadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 358738-57-5 Structure

  • Basic information

    1. Product Name: 3,5-bis(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-1,2,4-thiadiazole
    2. Synonyms: 3,5-bis(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-1,2,4-thiadiazole
    3. CAS NO:358738-57-5
    4. Molecular Formula:
    5. Molecular Weight: 1243.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 358738-57-5.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: 3,5-bis(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-1,2,4-thiadiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-bis(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-1,2,4-thiadiazole(358738-57-5)
    11. EPA Substance Registry System: 3,5-bis(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-1,2,4-thiadiazole(358738-57-5)

  • 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: 358738-57-5(Hazardous Substances Data)

358738-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 358738-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,8,7,3 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 358738-57:
(8*3)+(7*5)+(6*8)+(5*7)+(4*3)+(3*8)+(2*5)+(1*7)=195
195 % 10 = 5
So 358738-57-5 is a valid CAS Registry Number.

358738-57-5Downstream Products

358738-57-5Relevant articles and documents

Preparation of 3,5-bis-(β-D-glycopyranosyl)-1,2,4-thiadiazoles from C-(β-D-glycopyranosyl)thioformamides

Osz,Czifrák,Deim,Szilágyi,Bényei,Somsák

, p. 5429 - 5434 (2007/10/03)

Acylated C-glycopyranosyl thioformamides of D-gluco, D-galacto, and D-xylo configuration were obtained by treating the corresponding glycosyl cyanides with hydrogen sulfide in the presence of triethylamine. The thioformamides gave 3,5-bis-(β-D-glycopyranosyl)-1,2,4-thiadiazoles in reactions with potassium bromate and sodium dithionite in dichloromethane-water biphasic solvent mixture. Deprotected derivatives were prepared by Zemple?n deacylation.

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