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3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 39078-08-5 Structure
  • Basic information

    1. Product Name: 3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-ene
    2. Synonyms:
    3. CAS NO:39078-08-5
    4. Molecular Formula: C6H6O2
    5. Molecular Weight: 110.1106
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 39078-08-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 179°C at 760 mmHg
    3. Flash Point: 55.3°C
    4. Appearance: N/A
    5. Density: 1.387g/cm3
    6. Vapor Pressure: 1.3mmHg at 25°C
    7. Refractive Index: 1.584
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-ene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-ene(39078-08-5)
    12. EPA Substance Registry System: 3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-ene(39078-08-5)
  • 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: 39078-08-5(Hazardous Substances Data)

39078-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39078-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,7 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39078-08:
(7*3)+(6*9)+(5*0)+(4*7)+(3*8)+(2*0)+(1*8)=135
135 % 10 = 5
So 39078-08-5 is a valid CAS Registry Number.

39078-08-5Relevant articles and documents

Synthesis of novel mono and bis-indole conduritol derivatives and their α/β-glycosidase inhibitory effects

Cavdar, Hueseyin,Talaz, Oktay,Ekinci, Deniz

, p. 7499 - 7503 (2013/02/22)

Here we synthesized four novel indole conduritol derivatives 1-4 for the first time in the literature and probed their biological activities with the α and β-glucosidases. The compounds showed quite effective glucosidase inhibitory action. IC50

Synthesis of novel cyano-cyclitols and their stereoselective biotransformation catalyzed by Rhodococcus erythropolis A4

D'Antona, Nicola,Nicolosi, Giovanni,Morrone, Raffaele,Kubac, David,Kaplan, Ondrej,Martinkova, Ludmila

experimental part, p. 695 - 702 (2010/08/03)

A variety of novel cyano-cyclitols possessing complex stereochemistry have been synthesized. These compounds were subjected to the biocatalyzed hydrolysis of their nitrile groups. The bacterial strain Rhodococcus erythropolis A4, expressing a nitrile hydr

A novel chemo-multienzymatic synthesis of bioactive cyclophellitol and epi-cyclophellitol in both enantiopure forms

D'Antona, Nicola,Morrone, Raffaele,Bovicelli, Paolo,Gambera, Giovanni,Kubac, David,Martinkova, Ludmila

scheme or table, p. 2448 - 2454 (2011/02/22)

A new route to synthesize cyclophellitol and epi-cyclophellitol from racemic starting materials in enantiopure forms has been developed. The synthesis involves a multi-enzymatic biotransformation pathway of the novel cyano-cyclitol (1R,4S,5R,6R)/(1S,4R,5S

Concerning the reaction of anti-benzene dioxide with various nucleophiles

Esser, Thomas,Farkas, Frederic,Mangholz, Sissi,Sequin, Urs

, p. 3709 - 3720 (2007/10/02)

trans-3,4:5,6-Diepoxycyclohex-1-ene (anti-benzene dioxide) (5) was brought into reaction with several S, O, and C nucleophiles. S and O nucleophiles gave the bis-adducts stemming from independent reaction of the two epoxy functions. C nucleophiles, on the

cis-/trans--Trithia- and trans--Hexathia-tris-?-homobenzenes

Kagabu, Shinzo,Kaiser, Clemens,Keller, Reinhold,Becker, Paul G.,Mueller, Klaus-Helmuth,et. al.

, p. 741 - 756 (2007/10/02)

Starting from the cis- and trans-benzene trioxides 2/7 the cis-/trans--Trithia-tris-?-homobenzenes 1/6 and the trans-dioxathia-/oxadithia analogs 19/21 are synthesized by regioselective epoxide opening reactions with appropriate S-nucleophiles.Under the influence of heat and light cis-trisulfide 1 quickly looses sulfur and does not undergo ?2+?2+?2>cycloreversion.Attempts to build up cis--tris-?-homobenzenes from 2 by threefold six-membered ring anellation, in the special case of 1,2-benzenedithiol as 1,4-dinucleophil, led preferably to the trans--hexathia-tris-?-homobenzene 44 (X-ray analysis) manifesting effective S-neighbouring group participation. cis-Trisulfide 1 is a poor tridentate ligand: only with Ni(ClO4)2 a 2:1 complex (presumably octahedral, 48) is formed.

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