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CAS

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316806-88-9

1L-2,3,4,5-tetra-O-benzyl-chiro-inositol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 316806-88-9 Structure

  • Basic information

    1. Product Name: 1L-2,3,4,5-tetra-O-benzyl-chiro-inositol
    2. Synonyms: 1L-2,3,4,5-tetra-O-benzyl-chiro-inositol
    3. CAS NO:316806-88-9
    4. Molecular Formula:
    5. Molecular Weight: 540.656
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 316806-88-9.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: 1L-2,3,4,5-tetra-O-benzyl-chiro-inositol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1L-2,3,4,5-tetra-O-benzyl-chiro-inositol(316806-88-9)
    11. EPA Substance Registry System: 1L-2,3,4,5-tetra-O-benzyl-chiro-inositol(316806-88-9)

  • 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: 316806-88-9(Hazardous Substances Data)

316806-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 316806-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,6,8,0 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 316806-88:
(8*3)+(7*1)+(6*6)+(5*8)+(4*0)+(3*6)+(2*8)+(1*8)=149
149 % 10 = 9
So 316806-88-9 is a valid CAS Registry Number.

316806-88-9Relevant articles and documents

L-chiro-inositol derivatives from myo-inositol. Building blocks for inositolphosphoglycans

Cid, M. Belén,Alfonso, Francisco,Martín-Lomas, Manuel

, p. 1370 - 1372 (2007/10/03)

A straightforward synthesis of L-chiro-inositol, deoxy L-chiro-inositol derivatives and L-chiro-inositol building blocks for the preparation of inositolphosphoglycans, is reported from myoinositol. Glycosylation with 2-azido-3,4,6-tri-O-benzyl-2-deoxy-D-g

New syntheses of 1D- and 1L-1,2-anhydro-myo-inositol and assessment of their glycosidase inhibitory activities

Falshaw, Andrew,Hart, Joanne B.,Tyler, Peter C.

, p. 301 - 308 (2007/10/03)

The 1D and 1L enantiomers of 1,2-anhydro-myo-inositol (conduritol B epoxide) were synthesised from 1d-pinitol and 1l-quebrachitol, respectively, and their activities were compared in selected glycosidase inhibition assays. The 1d enantiomer was found to be the active isomer, functioning as an irreversible inhibitor of sweet almond β-D-glucosidase. Neither isomer was active against the α-D-glucosidase from Bacillus stearothermophilus or the β-D-galactosidase from Aspergillus oryzae. (C) 2000 Elsevier Science Ltd.

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