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3-(3,5-dimethylphenyl)-4H-1-benzopyran-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1017079-86-5 Structure
  • Basic information

    1. Product Name: 3-(3,5-dimethylphenyl)-4H-1-benzopyran-4-one
    2. Synonyms: 3-(3,5-dimethylphenyl)-4H-1-benzopyran-4-one
    3. CAS NO:1017079-86-5
    4. Molecular Formula:
    5. Molecular Weight: 250.297
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1017079-86-5.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-(3,5-dimethylphenyl)-4H-1-benzopyran-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(3,5-dimethylphenyl)-4H-1-benzopyran-4-one(1017079-86-5)
    11. EPA Substance Registry System: 3-(3,5-dimethylphenyl)-4H-1-benzopyran-4-one(1017079-86-5)
  • 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: 1017079-86-5(Hazardous Substances Data)

1017079-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1017079-86-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,7,0,7 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1017079-86:
(9*1)+(8*0)+(7*1)+(6*7)+(5*0)+(4*7)+(3*9)+(2*8)+(1*6)=135
135 % 10 = 5
So 1017079-86-5 is a valid CAS Registry Number.

1017079-86-5Downstream Products

1017079-86-5Relevant articles and documents

A novel synthesis of isoflavones via copper(I)-catalyzed intramolecular cyclization reaction

Li, Qiu-Lian,Liu, Qi-Lun,Ge, Zhi-Yuan,Zhu, Yong-Ming

experimental part, p. 1304 - 1309 (2011/09/15)

Isoflavone derivatives were synthesized via intramolecular cyclization of 3-(2-bromophenyl)-3-oxopropanal derivatives, using CuI as the catalyst, 2-picolinic acid (=pyridine-2-carboxylic acid) as the ligand, K 2CO3 as the base, and DMF as the solvent, in up to 96% yield. The synthesis is functional group-tolerant. Copyright

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