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1431934-83-6

ethyl 6-methyl-3-(4-nitrophenyl)-2H-1,4-oxazine-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1431934-83-6 Structure

  • Basic information

    1. Product Name: ethyl 6-methyl-3-(4-nitrophenyl)-2H-1,4-oxazine-5-carboxylate
    2. Synonyms: ethyl 6-methyl-3-(4-nitrophenyl)-2H-1,4-oxazine-5-carboxylate
    3. CAS NO:1431934-83-6
    4. Molecular Formula:
    5. Molecular Weight: 290.276
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1431934-83-6.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: ethyl 6-methyl-3-(4-nitrophenyl)-2H-1,4-oxazine-5-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 6-methyl-3-(4-nitrophenyl)-2H-1,4-oxazine-5-carboxylate(1431934-83-6)
    11. EPA Substance Registry System: ethyl 6-methyl-3-(4-nitrophenyl)-2H-1,4-oxazine-5-carboxylate(1431934-83-6)

  • 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: 1431934-83-6(Hazardous Substances Data)

1431934-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1431934-83-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,1,9,3 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1431934-83:
(9*1)+(8*4)+(7*3)+(6*1)+(5*9)+(4*3)+(3*4)+(2*8)+(1*3)=156
156 % 10 = 6
So 1431934-83-6 is a valid CAS Registry Number.

1431934-83-6Downstream Products

1431934-83-6Relevant articles and documents

Azirinium ylides from α-diazoketones and 2H-azirines on the route to 2H-1,4-oxazines: Three-membered ring opening vs 1,5-cyclization

Rostovskii, Nikolai V.,Novikov, Mikhail S.,Khlebnikov, Alexander F.,Starova, Galina L.,Avdontseva, Margarita S.

, p. 302 - 312 (2015)

Strained azirinium ylides derived from 2H-azirines and α-diazoketones under Rh(II)-catalysis can undergo either irreversible ring opening across the N-C2 bond to 2-azabuta-1,3-dienes that further cyclize to 2H-1,4-oxazines or reversibly undergo a 1,5-cycl

Rh(II)-carbenoid mediated 2H-azirine ring-expansion as a convenient route to non-fused photo- and thermochromic 2H-1,4-oxazines

Rostovskii, Nikolai V.,Novikov, Mikhail S.,Khlebnikov, Alexander F.,Khlebnikov, Vsevolod A.,Korneev, Sergei M.

, p. 4292 - 4301 (2013/06/27)

The Rh2(OAc)4-catalyzed domino reaction of 2H-azirines with 2-acyl-2-diazoacetates provides a unique synthetic approach to non-fused 2H-1,4-oxazines. The reaction proceeds via sequential formation of a rhodium carbenoid, an azirinium

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