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871125-77-8

2-(4'-methoxybenzyloxy)phenylboronic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 871125-77-8 Structure

  • Basic information

    1. Product Name: 2-(4'-methoxybenzyloxy)phenylboronic acid
    2. Synonyms: Boronicacid, [2-(4-methoxyphenoxy)phenyl]- (9CI)
    3. CAS NO:871125-77-8
    4. Molecular Formula: C13H13 B O4
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 871125-77-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(4'-methoxybenzyloxy)phenylboronic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4'-methoxybenzyloxy)phenylboronic acid(871125-77-8)
    11. EPA Substance Registry System: 2-(4'-methoxybenzyloxy)phenylboronic acid(871125-77-8)

  • 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: 871125-77-8(Hazardous Substances Data)

871125-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 871125-77-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,1,2 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 871125-77:
(8*8)+(7*7)+(6*1)+(5*1)+(4*2)+(3*5)+(2*7)+(1*7)=168
168 % 10 = 8
So 871125-77-8 is a valid CAS Registry Number.

871125-77-8Downstream Products

871125-77-8Relevant articles and documents

Ag-Catalyzed Cyclization of Arylboronic Acids with Elemental Selenium for the Synthesis of Selenaheterocycles

Gao, Wen-Xia,Huang, Xiao-Bo,Liu, Miao-Chang,Wu, Hua-Yue,Zhang, Xue,Zhou, Yun-Bing

, p. 5639 - 5644 (2020/11/30)

A general method for the synthesis of five-membered and six-membered selenaheterocycles through Ag-catalyzed C?Se bond-forming reaction is reported. This reaction proceeds via intramolecular cyclization of arylboronic acids with selenium powder. Preliminary mechanism studies demonstrate that this transformation involves a selenium-centred radical intermediate. (Figure presented.).

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