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CAS

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1446350-88-4

11-(4-nitrophenyl)-2,3-dihydrobenzo[g]cyclopenta[b]chromene-1,5,10(11H)-trione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446350-88-4 Structure

  • Basic information

    1. Product Name: 11-(4-nitrophenyl)-2,3-dihydrobenzo[g]cyclopenta[b]chromene-1,5,10(11H)-trione
    2. Synonyms: 11-(4-nitrophenyl)-2,3-dihydrobenzo[g]cyclopenta[b]chromene-1,5,10(11H)-trione
    3. CAS NO:1446350-88-4
    4. Molecular Formula:
    5. Molecular Weight: 387.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446350-88-4.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: 11-(4-nitrophenyl)-2,3-dihydrobenzo[g]cyclopenta[b]chromene-1,5,10(11H)-trione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 11-(4-nitrophenyl)-2,3-dihydrobenzo[g]cyclopenta[b]chromene-1,5,10(11H)-trione(1446350-88-4)
    11. EPA Substance Registry System: 11-(4-nitrophenyl)-2,3-dihydrobenzo[g]cyclopenta[b]chromene-1,5,10(11H)-trione(1446350-88-4)

  • 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: 1446350-88-4(Hazardous Substances Data)

1446350-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446350-88-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,3,5 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1446350-88:
(9*1)+(8*4)+(7*4)+(6*6)+(5*3)+(4*5)+(3*0)+(2*8)+(1*8)=164
164 % 10 = 4
So 1446350-88-4 is a valid CAS Registry Number.

1446350-88-4Downstream Products

1446350-88-4Relevant articles and documents

Efficient and green syntheses of 12-aryl-2,3,4,12-tetrahydrobenzo[b] xanthene-1,6,11-triones in water and task-specific ionic liquid

Khurana, Jitender M.,Lumb, Anshika,Chaudhary, Ankita,Nand, Bhaskara

, p. 2147 - 2154 (2013)

Facile and convenient one-pot cascade/tandem approaches for the syntheses of privileged medicinal scaffolds, 12-aryl-2,3,4,12-tetrahydrobenzo[b]xanthene- 1,6,11-trione derivatives, have been reported under extremely mild reaction conditions using a catalytic amount of H2SO4 in water or in the presence of the acidic ionic liquid bmim[HSO4], which could be recycled. Copyright

Multicomponent synthesis of some benzo, pyrimido and pyrazolo fused heterocycles using [Nmp]H2Po4 as an efficient reaction medium

Kumari, Sudesh,Khurana

, p. 395 - 404 (2019/01/21)

An efficient synthesis of benzoxanthene, pyrimidoquinoline, pyrimidochromene and pyrazolopyridine fused heterocycles by condensation of aromatic aldehydes, 2- hydroxy-1,4-naphthoquinone/ 6-amino-1,3-dimethyl uracil/ 1,3-dimethyl barbituric acid/ 5-amino-3-methyl-1-phenylpyrazole and 5,5-dimethylcyclohexane-1,3-dione/5- methylcyclohexane-1,3-dione/ cyclohexane-1,3-dione/cyclopentane-1,3-dione has been developed using [NMP]H2PO4 as a highly efficient reaction medium and catalyst. All the reactions proceeded smoothly and gave corresponding products in high yield after a simple workup.

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