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CAS

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133147-62-3

1α,5α,6β-1-benzoyl-6-morpholino-bicyclo<3.1.0>hexane-6-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133147-62-3 Structure

  • Basic information

    1. Product Name: 1α,5α,6β-1-benzoyl-6-morpholino-bicyclo<3.1.0>hexane-6-carbonitrile
    2. Synonyms: 1α,5α,6β-1-benzoyl-6-morpholino-bicyclo<3.1.0>hexane-6-carbonitrile
    3. CAS NO:133147-62-3
    4. Molecular Formula:
    5. Molecular Weight: 296.369
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133147-62-3.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: 1α,5α,6β-1-benzoyl-6-morpholino-bicyclo<3.1.0>hexane-6-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1α,5α,6β-1-benzoyl-6-morpholino-bicyclo<3.1.0>hexane-6-carbonitrile(133147-62-3)
    11. EPA Substance Registry System: 1α,5α,6β-1-benzoyl-6-morpholino-bicyclo<3.1.0>hexane-6-carbonitrile(133147-62-3)

  • 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: 133147-62-3(Hazardous Substances Data)

133147-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133147-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,1,4 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133147-62:
(8*1)+(7*3)+(6*3)+(5*1)+(4*4)+(3*7)+(2*6)+(1*2)=103
103 % 10 = 3
So 133147-62-3 is a valid CAS Registry Number.

133147-62-3Relevant articles and documents

FUNCTIONALIZED CHLOROENAMINES IN AMINOCYCLOPROPANE SYNTHESIS - V. SYNTHESIS AND REACTIONS OF AMINOCYCLOPROPYLKETONES

Vilsmaier, Elmar,Doerrenbaecher, Ralph,Mueller, Lutz

, p. 8103 - 8116 (2007/10/02)

Conjugated acylated chloroenamines 5A,C were available by chlorination of mixtures of acylated enamines 8A,C/9A,C by NCS at 0 deg C.Nonconjugated chloroenamines 10Aa and 10Ba could be obtained by NCS-chlorination of the conjugated acylenamines 9A,B at low temperature.Reaction of 5Aa-5Ac, 5Ae, 5Af with cyanide produced morpholinocyclopropylketones 11A.In two cases aminofurans 12Ad and 12Ca resulted as products of this reaction.More generally amino-aryl-furans 12 were formed by thermolysis of the aryl-cyclopropylketones 11.Amino-alkyl-furans as 12Ae and 12Af only could be trapped by a Diels-Alder reaction leading to 16Ae and 16Af.Epoxyenamines 29A,B unexpectedly were produced from the interaction of cyanide with the chloroenamines 10Aa and 10Ba.

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