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3,7-dimethyl-10-(4-cyanophenyl)-1H,9H,10H-dipyrano[4,3-b:3,4-e]pyran-1,9-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1190374-94-7 Structure
  • Basic information

    1. Product Name: 3,7-dimethyl-10-(4-cyanophenyl)-1H,9H,10H-dipyrano[4,3-b:3,4-e]pyran-1,9-dione
    2. Synonyms:
    3. CAS NO:1190374-94-7
    4. Molecular Formula:
    5. Molecular Weight: 347.327
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1190374-94-7.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: 3,7-dimethyl-10-(4-cyanophenyl)-1H,9H,10H-dipyrano[4,3-b:3,4-e]pyran-1,9-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,7-dimethyl-10-(4-cyanophenyl)-1H,9H,10H-dipyrano[4,3-b:3,4-e]pyran-1,9-dione(1190374-94-7)
    11. EPA Substance Registry System: 3,7-dimethyl-10-(4-cyanophenyl)-1H,9H,10H-dipyrano[4,3-b:3,4-e]pyran-1,9-dione(1190374-94-7)
  • 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: 1190374-94-7(Hazardous Substances Data)

1190374-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1190374-94-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,3,7 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1190374-94:
(9*1)+(8*1)+(7*9)+(6*0)+(5*3)+(4*7)+(3*4)+(2*9)+(1*4)=157
157 % 10 = 7
So 1190374-94-7 is a valid CAS Registry Number.

1190374-94-7Downstream Products

1190374-94-7Relevant articles and documents

Ionic liquid promoted and mediated green preparation of arylbispyranylmethane and pyran derivatives and their hybrid with a pyrimidine nucleoside

Zhang, Xinying,Qu, Yingying,Fan, Xuesen,Wang, Xia,Wang, Jianji

, p. 473 - 477 (2009)

The utilisation of an ionic liquid-[bmim][BF4] as both reaction medium and promoter for the reaction between aldehyde and 4-hydroxy-6- methylpyran-2-one is described. Without any added catalyst, this reaction was realised efficiently to give arylbispyranylmethane derivatives in high yields. Alternatively, when this reaction was carried out in the presence of acetic anhydride, fused pyran derivatives were obtained. These two novel procedures have advantages such as an environmentally benign nature, high efficiency, simple operation process and mild reaction conditions. As an application, these procedures were used in the preparation of novel 5-substituted pyrimidine nucleoside derivatives with potential antiviral activities.

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