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2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-6-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

220658-29-7

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  • 220658-29-7 Structure

  • Basic information

    1. Product Name: 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-6-carboxylic acid
    2. Synonyms: 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-6-carboxylic acid
    3. CAS NO:220658-29-7
    4. Molecular Formula:
    5. Molecular Weight: 396.44
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-6-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-6-carboxylic acid(220658-29-7)
    11. EPA Substance Registry System: 2-<2-<3-(tert-butyl)oxycarbonyl-1-propyloxy>phenyl>benzofuran-6-carboxylic acid(220658-29-7)

  • 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: 220658-29-7(Hazardous Substances Data)

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220658-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220658-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,6,5 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 220658-29:
(8*2)+(7*2)+(6*0)+(5*6)+(4*5)+(3*8)+(2*2)+(1*9)=117
117 % 10 = 7
So 220658-29-7 is a valid CAS Registry Number.

220658-29-7Relevant academic research and scientific papers

A convenient synthesis of 2-phenylbenzofuran derivatives with potent testosterone 5α-reductase inhibitory activities

Ishibashi, Koki,Nakajima, Katsuyoshi,Nishi, Takahide

, p. 2669 - 2675 (2007/10/03)

A convenient method for the synthesis of 4-[2-(benzo[b]furan-2-yl)phenyloxy]butyric acid derivatives with a carbamoyl group at the 5 or 6 position of the benzofuran ring showing potent 5α-reductase inhibitory activities was developed. Oxazolin-2-ylbenzofu

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