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CAS

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87520-10-3

cycletanide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 87520-10-3 Structure

  • Basic information

    1. Product Name: cycletanide
    2. Synonyms: cycletanide
    3. CAS NO:87520-10-3
    4. Molecular Formula: C14H12ClNO2
    5. Molecular Weight: 261.70358
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87520-10-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: cycletanide(CAS DataBase Reference)
    10. NIST Chemistry Reference: cycletanide(87520-10-3)
    11. EPA Substance Registry System: cycletanide(87520-10-3)

  • 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: 87520-10-3(Hazardous Substances Data)

87520-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87520-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,2 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87520-10:
(7*8)+(6*7)+(5*5)+(4*2)+(3*0)+(2*1)+(1*0)=133
133 % 10 = 3
So 87520-10-3 is a valid CAS Registry Number.

87520-10-3Downstream Products

87520-10-3Relevant articles and documents

Separation of isomers of furo (3,4-C) pyridine derivatives

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, (2008/06/13)

This invention relates to a method for the separation of stereoisomers of 7-hydroxy-furo[3,4-c]pyridine derivatives of the formula STR1 wherein R3, R4 and R6 represent various substitutents, which comprises reacting a fully O-acetylated monosaccharide halogenide with a racemate of the selected 7-hydroxy-furo[3,4-c]pyridine derivative, to form the (+) and (-) (O-acetylated monosaccharide) (furo[3,4-c] pyridine 7-yl derivative) ethers, then separating the (+) and the (-) ethers by selective crystallization, in an hydroalcoholic medium, either of the acetylated forms or of the corresponding desacetylated forms and, finally, working up each of the separated derivatives by the usual routes. The compounds are known pharmaceuticals.

Stereospecific process for the preparation of furo[3,4-c]pyridine, enantiomer, compounds thus obtained and therapeutical compositions thereof

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, (2008/06/13)

The present invention relates to stereospecific processes for the preparation of enantiomers of 3-substituted-furo[3,4-c]pyridine of formula I, wherein R3, R4 and R6 stand for various substituents, comprising the steps of:

Furo-(3,4-c)-pyridine derivatives and their pharmaceutical use

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, (2008/06/13)

This invention relates to new 1,3-dihydro-6-methyl-7-hydroxy-furo-(3,4-c)-pyridine derivatives of the general formula STR1 wherein A2)n --, n being an integer of from 1 to 5, or a homocyclic o

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