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863036-13-9

6-Benzofuranol, 2,7-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 863036-13-9 Structure

  • Basic information

    1. Product Name: 6-Benzofuranol, 2,7-dimethyl-
    2. Synonyms: 6-Benzofuranol, 2,7-dimethyl-
    3. CAS NO:863036-13-9
    4. Molecular Formula: C10H10O2
    5. Molecular Weight: 162.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 863036-13-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 166.0±10.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.181±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 9.41±0.50(Predicted)
    10. CAS DataBase Reference: 6-Benzofuranol, 2,7-dimethyl-(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-Benzofuranol, 2,7-dimethyl-(863036-13-9)
    12. EPA Substance Registry System: 6-Benzofuranol, 2,7-dimethyl-(863036-13-9)

  • 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: 863036-13-9(Hazardous Substances Data)

863036-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863036-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,0,3 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 863036-13:
(8*8)+(7*6)+(6*3)+(5*0)+(4*3)+(3*6)+(2*1)+(1*3)=159
159 % 10 = 9
So 863036-13-9 is a valid CAS Registry Number.

863036-13-9Upstream product

863036-13-9Downstream Products

863036-13-9Relevant articles and documents

An efficient solid-phase synthesis of substituted benzofuran using selenium-bound resin

Zhang, Yin Jun,Wang, Yu Guang

experimental part, p. 212 - 216 (2012/07/13)

A very efficient solid-phase synthesis of substituted benzofuran using polymer-supported selenium resin is described. The advantages of the new method are good yields, high purity, straightforward operations, broad range and high diversity of products, lack of odor, and good stability of the resins. The easy work-up procedure makes the method suitable for building parallel libraries.

Facile construction of the benzofuran and chromene ring systems via Pd II-catalyzed oxidative cyclization

So, Won Youn,Jeong, Im Eom

, p. 3355 - 3358 (2007/10/03)

(Chemical Equation Presented) We herein report the development of one-pot procedures for the conversion of allyl aryl ethers to 2-methylbenzofurans (via sequential Claisen rearrangement and oxidative cyclization) and for the conversion of aryl homoallyl e

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