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CAS

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727651-34-5

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

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  • 727651-34-5 Structure

  • Basic information

    1. Product Name: 1-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-5-bromoindole
    2. Synonyms: 1-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-5-bromoindole
    3. CAS NO:727651-34-5
    4. Molecular Formula:
    5. Molecular Weight: 718.687
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 727651-34-5.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: 1-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-5-bromoindole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-5-bromoindole(727651-34-5)
    11. EPA Substance Registry System: 1-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-5-bromoindole(727651-34-5)

  • 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: 727651-34-5(Hazardous Substances Data)

727651-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 727651-34-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,7,6,5 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 727651-34:
(8*7)+(7*2)+(6*7)+(5*6)+(4*5)+(3*1)+(2*3)+(1*4)=175
175 % 10 = 5
So 727651-34-5 is a valid CAS Registry Number.

727651-34-5Relevant articles and documents

Synthesis and antiproliferative activities of diversely substituted glycosyl-isoindigo derivatives

Sassatelli, Mathieu,Bouchikhi, Fadoua,Messaoudi, Samir,Anizon, Fabrice,Debiton, Eric,Barthomeuf, Chantal,Prudhomme, Michelle,Moreau, Pascale

, p. 88 - 100 (2007/10/03)

In the course of structure-activity relationship studies, diversely substituted 1-(β-D-glucopyranosyl)-isoindigo derivatives were prepared from commercially available indolines. Their antiproliferative activities were evaluated toward a panel of human solid cancer cell lines (PC 3, DLD-1, MCF-7, M4Beu, A549, PA 1), a murine cell line (L929) and a human fibroblast primary culture to get an insight into the substitution pattern required for the best biological potencies.

Synthesis of glycosyl-isoindigo derivatives

Sassatelli, Mathieu,Saab, Elias,Anizon, Fabrice,Prudhomme, Michelle,Moreau, Pascale

, p. 4827 - 4830 (2007/10/03)

The synthesis of 1-(β-D-glucopyranosyl)-isoindigo from commercially available indoline is described. The synthetic pathway used allowed the substitution of the aromatic moiety by either electron donor or acceptor substituents.

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