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CAS

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638203-33-5

3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 638203-33-5 Structure

  • Basic information

    1. Product Name: 3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol
    2. Synonyms: 3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol
    3. CAS NO:638203-33-5
    4. Molecular Formula:
    5. Molecular Weight: 672.719
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 638203-33-5.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: 3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol(638203-33-5)
    11. EPA Substance Registry System: 3,4,5,6-tetra-O-benzyl-1-O-trifluoromethanesulfonyl-L-myo-inositol(638203-33-5)

  • 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: 638203-33-5(Hazardous Substances Data)

638203-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 638203-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,8,2,0 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 638203-33:
(8*6)+(7*3)+(6*8)+(5*2)+(4*0)+(3*3)+(2*3)+(1*3)=145
145 % 10 = 5
So 638203-33-5 is a valid CAS Registry Number.

638203-33-5Relevant 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

Phosphatidyl inositol analogs useful as anti-inflammatory/analgesic agents

-

, (2008/06/13)

Phosphatidyl inositol analogs are found to be effective phospholipase C inhibitors and thereby potent anti-inflammatory and analgesic agents. These phosphatidyl inositol analogs are prepared by condensation of a protected inositol with a substituted phosphonic or phosphorous acid followed by removal of protecting groups.

Sulfonyl or carbonyl inositol derivatives useful as anti-inflammatory/analgesic agents

-

, (2008/06/13)

Sulfonyl or carbonyl derivatives of inositols are found to be effective phospholipase C inhibitors and thereby potent anti-inflammatory and analgesic agents. These inositol derivatives are prepared by condensation of a protected inositol with a substituted sulfonic or carboxylic acid derivative followed by removal of protecting groups.

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