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CAS

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1187735-29-0

3-(4-nitrophenyl)-5-(D-gluco-1,2,3,5-tetraacetoxy-4-hydroxypentyl)-1,2,4-oxadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1187735-29-0 Structure

  • Basic information

    1. Product Name: 3-(4-nitrophenyl)-5-(D-gluco-1,2,3,5-tetraacetoxy-4-hydroxypentyl)-1,2,4-oxadiazole
    2. Synonyms:
    3. CAS NO:1187735-29-0
    4. Molecular Formula:
    5. Molecular Weight: 509.427
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1187735-29-0.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-(4-nitrophenyl)-5-(D-gluco-1,2,3,5-tetraacetoxy-4-hydroxypentyl)-1,2,4-oxadiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-nitrophenyl)-5-(D-gluco-1,2,3,5-tetraacetoxy-4-hydroxypentyl)-1,2,4-oxadiazole(1187735-29-0)
    11. EPA Substance Registry System: 3-(4-nitrophenyl)-5-(D-gluco-1,2,3,5-tetraacetoxy-4-hydroxypentyl)-1,2,4-oxadiazole(1187735-29-0)

  • 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: 1187735-29-0(Hazardous Substances Data)

1187735-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1187735-29-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,7,7,3 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1187735-29:
(9*1)+(8*1)+(7*8)+(6*7)+(5*7)+(4*3)+(3*5)+(2*2)+(1*9)=190
190 % 10 = 0
So 1187735-29-0 is a valid CAS Registry Number.

1187735-29-0Downstream Products

1187735-29-0Relevant articles and documents

Glucose-based spiro-heterocycles as potent inhibitors of glycogen phosphorylase

Nagy, Veronika,Benltifa, Mahmoud,Vidal, Sebastien,Berzsenyi, Eszter,Teilhet, Cathie,Czifrak, Katalin,Batta, Gyula,Docsa, Tibor,Gergely, Pal,Somsak, Laszlo,Praly, Jean-Pierre

, p. 5696 - 5707 (2009)

Glucopyranosylidene-spiro-1,4,2-oxathiazoles were prepared in high yields by NBS-mediated spiro-cyclization of the corresponding glucosyl-hydroximothioates. In an effort to synthesize analogous glucopyranosylidene-spiro-1,2,4-oxadiazolines, with a nitrogen atom instead of the sulphur, attempted cyclizations resulted in aromatization of the heterocycle with opening of the pyranosyl ring. Enzymatic measurements showed that some of the glucose-based inhibitors were active in the micromolar range. The 2-naphthyl-substituted 1,4,2-oxathiazole displayed the best inhibition against RMGPb (Ki = 160 nM), among glucose-based inhibitors known to date.

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