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CAS

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1393931-59-3

(R)-diethyl 3-(2-chlorophenyl)-3,4-dihydrobenzo[b][1,4]oxazine-2,2-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1393931-59-3 Structure

  • Basic information

    1. Product Name: (R)-diethyl 3-(2-chlorophenyl)-3,4-dihydrobenzo[b][1,4]oxazine-2,2-dicarboxylate
    2. Synonyms:
    3. CAS NO:1393931-59-3
    4. Molecular Formula:
    5. Molecular Weight: 389.835
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393931-59-3.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: (R)-diethyl 3-(2-chlorophenyl)-3,4-dihydrobenzo[b][1,4]oxazine-2,2-dicarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-diethyl 3-(2-chlorophenyl)-3,4-dihydrobenzo[b][1,4]oxazine-2,2-dicarboxylate(1393931-59-3)
    11. EPA Substance Registry System: (R)-diethyl 3-(2-chlorophenyl)-3,4-dihydrobenzo[b][1,4]oxazine-2,2-dicarboxylate(1393931-59-3)

  • 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: 1393931-59-3(Hazardous Substances Data)

1393931-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393931-59-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,9,3 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1393931-59:
(9*1)+(8*3)+(7*9)+(6*3)+(5*9)+(4*3)+(3*1)+(2*5)+(1*9)=193
193 % 10 = 3
So 1393931-59-3 is a valid CAS Registry Number.

1393931-59-3Downstream Products

1393931-59-3Relevant articles and documents

Construction of functionalized 2,3-dihydro-1,4-benzoxazines via [5 + 1] annulations of 2-halo-1,3-dicarbonyl compounds with imines

Zhang, Ya-Ru,Xie, Jian-Wu,Huang, Xu-Jiao,Zhu, Wei-Dong

experimental part, p. 6554 - 6561 (2012/09/08)

A series of functionalized 2,3-dihydro-1,4-benzoxazines were obtained in moderate to excellent yields via domino [5 + 1] annulations of 2-halo-1,3-dicarbonyl compounds 2 with imines 1 under mild conditions and the application of this method in the synthesis of bioactive analogues, such as functionalized tetracyclic-1,4-benzoxazines which contain two new heterocyclic rings and one quaternary carbon center has also been developed.

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