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CAS

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86359-57-1

5H-Inden-5-one, 1,3a,4,6,7,7a-hexahydro-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86359-57-1 Structure

  • Basic information

    1. Product Name: 5H-Inden-5-one, 1,3a,4,6,7,7a-hexahydro-, cis-
    2. Synonyms:
    3. CAS NO:86359-57-1
    4. Molecular Formula: C9H12O
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86359-57-1.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: 5H-Inden-5-one, 1,3a,4,6,7,7a-hexahydro-, cis-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5H-Inden-5-one, 1,3a,4,6,7,7a-hexahydro-, cis-(86359-57-1)
    11. EPA Substance Registry System: 5H-Inden-5-one, 1,3a,4,6,7,7a-hexahydro-, cis-(86359-57-1)

  • 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: 86359-57-1(Hazardous Substances Data)

86359-57-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86359-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,5 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86359-57:
(7*8)+(6*6)+(5*3)+(4*5)+(3*9)+(2*5)+(1*7)=171
171 % 10 = 1
So 86359-57-1 is a valid CAS Registry Number.

86359-57-1Relevant articles and documents

ISOMERIC CIS-BICYCLONONADIENES

Gevorkyan, G. G.,Belikova, N. A.,Bobyleva, A. A.,Pekhk, T. I.,Anfilogova, S. N.,et al.

, p. 1583 - 1588 (2007/10/02)

cis-Bicyclonona-2,7-dienes and the corresponding 2,8-dienes were obtained by the isomerization of cis-bicyclonona-3,7-diene and dehydration of the cis-bicyclonon-7(8)-en-3-ols.The 13C and PMR spectra of the isomeric dienes were investigated, and their retention times in GLC analysis were determined.The reaction of cis-bicyclonona-3,7-diene with N-bromosuccinimide in aqueous DMSO and the reaction of cis-bicyclonona-2,7-diene with acetic acid were studied.

ADDITION OF HYDROGEN BROMIDE TO CIS-BICYCLONONA-3,7-DIENE. SYNTHESIS OF 5-BROMOBREXANE AND BREXAN-5-ONE

Dubitskaya, N. F.,Khaibullina, E. A.,Pekhk, T. I.,Grishin, Yu. K.,Belikova, N. A.,Bobyleva, A. A.

, p. 1589 - 1593 (2007/10/02)

The addition of hydrogen bromide to cis-bicyclonona-3,7-diene takes place preferentially but not selectively at the double bond of the six-membered ring.In the case of gaseous hydrogen bromide only bromobicyclononenes are formed, but with 48percent aqueous hydrobromic acid the reaction is accompanied by transannular cyclization and by the formation of endo- and exo-5-bromobrexanes (16-20percent).A method is proposed for the production of brexan-5-one.

HYDROBORATION AND OXYMERCURATION-DEMERCURATION OF CIS-BICYCLONONA-3,7-DIENE. SYNTHESIS OF CIS-BICYCLONONENONES

Arbuzov, V. A.,Pekhk, T. I.,Belikova, N. A.,Bobyleva, A. A.,Plate, A. F.

, p. 273 - 282 (2007/10/02)

Four isomeric cis-bicyclononenones were obtained from cis-bicyclonona-3,7-diene by hydroboration and oxymercuration-demercuration.Their structures were determined by means of their 13C NMR spectra.The addition of the hydroborating agents takes place preferentially (60-80percent) at the cyclopentene double bond at the C7 and C8 atoms and is most selective in the case of 9-borabicyclononane.The direction of addition of mercuric acetate depends on the solvent; the reaction takes place most selectively (95percent) at the cyclohexene double bond in 1:9 aqueous THF, and here the mercury adds to the C4 carbon atom to the extent of 90percent.

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