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7-chloro-1,2-dihydrocyclopenta[b]indol-3(4H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 441067-87-4 Structure
  • Basic information

    1. Product Name: 7-chloro-1,2-dihydrocyclopenta[b]indol-3(4H)-one
    2. Synonyms: 7-chloro-1,2-dihydrocyclopenta[b]indol-3(4H)-one;7-Chloro-1,4-dihydro-2H-cyclopenta[b]indol-3-one
    3. CAS NO:441067-87-4
    4. Molecular Formula: C11H8ClNO
    5. Molecular Weight: 205.64032
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 441067-87-4.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: 7-chloro-1,2-dihydrocyclopenta[b]indol-3(4H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-chloro-1,2-dihydrocyclopenta[b]indol-3(4H)-one(441067-87-4)
    11. EPA Substance Registry System: 7-chloro-1,2-dihydrocyclopenta[b]indol-3(4H)-one(441067-87-4)
  • 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: 441067-87-4(Hazardous Substances Data)

441067-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 441067-87-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,1,0,6 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 441067-87:
(8*4)+(7*4)+(6*1)+(5*0)+(4*6)+(3*7)+(2*8)+(1*7)=134
134 % 10 = 4
So 441067-87-4 is a valid CAS Registry Number.

441067-87-4Relevant articles and documents

Tetracyclic compounds from cyclopent[b]indoles. Synthesis of isoxazolo[3′,4′:5,4]cyclopent[b]indoles

Sangeetha,Prasad, K.J. Rajendra

, p. 65 - 70 (2007/10/03)

Cyclopentan-1′,2′-dione-1′-arylhydrazones 3 obtained from the Japp-Klingemann reaction of diazotised aniline derivatives 1 and 2-hydroxymethylenecyclopentanone 2 on acid catalysed cyclization afforded cyclopent[b]indoles 4. These on mixed aldol condensati

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