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3,8-Bis(p-tolylsulfonyl)-(1α,2α,4α,7α)-3,8-diazatricyclo<5.1.0.02,4>oct-5-en is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54724-82-2 Structure
  • Basic information

    1. Product Name: 3,8-Bis(p-tolylsulfonyl)-(1α,2α,4α,7α)-3,8-diazatricyclo<5.1.0.02,4>oct-5-en
    2. Synonyms:
    3. CAS NO:54724-82-2
    4. Molecular Formula:
    5. Molecular Weight: 416.522
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54724-82-2.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: 3,8-Bis(p-tolylsulfonyl)-(1α,2α,4α,7α)-3,8-diazatricyclo<5.1.0.02,4>oct-5-en(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,8-Bis(p-tolylsulfonyl)-(1α,2α,4α,7α)-3,8-diazatricyclo<5.1.0.02,4>oct-5-en(54724-82-2)
    11. EPA Substance Registry System: 3,8-Bis(p-tolylsulfonyl)-(1α,2α,4α,7α)-3,8-diazatricyclo<5.1.0.02,4>oct-5-en(54724-82-2)
  • 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: 54724-82-2(Hazardous Substances Data)

54724-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54724-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54724-82:
(7*5)+(6*4)+(5*7)+(4*2)+(3*4)+(2*8)+(1*2)=132
132 % 10 = 2
So 54724-82-2 is a valid CAS Registry Number.

54724-82-2Relevant articles and documents

cis,trans-Oxaaza-bis-?-homobenzenes - 4H-1,4-Oxazocines

Mueller, Klaus-Helmut,Kaiser, Clemens,Pillat, Michael,Zipperer, Bernhard,Froom, Manfred,et al.

, p. 2492 - 2523 (2007/10/02)

The cis-oxaaza-bis-?-homobenzene framework has been synthesised via two routes starting from readily accessible materials (11, 25).As expected the N-SO2R derivatives 3a,b are sufficiently stable to be isolated; on heating, they readily and quantitatively undergo ?2 + ?2 + ?2>-cycloreversion to the 4H-1,4-oxazocines 6a,b (3b: t1/2(60 deg C) = 33.2 min; ΔG* = 104.0 kJ*mol-1).The latter prefer a non-planar, folded conformation.Using a precursor of 3b (27a), the thermally stable trans-oxaaza-bis-?-homobenzene 9 was obtained in very small yield (2 - 6percent) by two alternative pathways.

"cis-Diaza-bis-?-homobenzenes" (?2s + ?2s + ?2s>-Cycloreversion) - 1,4-Dihydro-1,4-diazocines ("Aromaticity")

Breuninger, Manfred,Schwesinger, Reinhard,Gallenkamp, Bernd,Mueller, Klaus-Helmut,Fritz, Hans,et al.

, p. 3161 - 3186 (2007/10/02)

Starting from "cis-benzene triimine" (3) the N,N'-disubstituted derivatives 8b-f are synthesized in 90-40percent yield.Nitrosation to the N-nitroso compounds 10b-f, spectroscopically identified below -30 deg C, and N2O-elimination lead to the c

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