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2'-benzyloxy-3-chloro-2-nitrobiphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1133877-04-9 Structure
  • Basic information

    1. Product Name: 2'-benzyloxy-3-chloro-2-nitrobiphenyl
    2. Synonyms: 2'-benzyloxy-3-chloro-2-nitrobiphenyl
    3. CAS NO:1133877-04-9
    4. Molecular Formula:
    5. Molecular Weight: 339.778
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1133877-04-9.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: 2'-benzyloxy-3-chloro-2-nitrobiphenyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2'-benzyloxy-3-chloro-2-nitrobiphenyl(1133877-04-9)
    11. EPA Substance Registry System: 2'-benzyloxy-3-chloro-2-nitrobiphenyl(1133877-04-9)
  • 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: 1133877-04-9(Hazardous Substances Data)

1133877-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1133877-04-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,3,8,7 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1133877-04:
(9*1)+(8*1)+(7*3)+(6*3)+(5*8)+(4*7)+(3*7)+(2*0)+(1*4)=149
149 % 10 = 9
So 1133877-04-9 is a valid CAS Registry Number.

1133877-04-9Relevant articles and documents

Suzuki-Miyaura cross-coupling of 2-nitroarenediazonium tetrafluoroborates: Synthesis of unsymmetrical 2-nitrobiphenyls and highly functionalized carbazoles

Kuethe, Jeffrey T.,Childers, Karla G.

, p. 1577 - 1586 (2008)

The Suzuki-Miyaura cross-coupling of 2-nitrodiazonium tetrafluoroborate salts with substituted boronic acids is an effective and efficient means of preparing highly functionalized 2-nitrobiphenyls in modest to excellent yield under extremely mild reaction conditions. Cross-coupling of 2-nitrodiazonium tetrafluoroborate salts with ortho-methoxy- and benzyloxyphenylboronic acids was also demonstrated leading to the ortho-ortho-2-nitrobiphenyls. Reductive cyclization of the 2-nitrobiphenyl products allows for the overall three-step synthesis of uniquely substituted carbazoles from readily available 2-nitroanilines. The methodology was further highlighted by the short total synthesis of the carbazole alkaloids clausine V, N, C, and glycoborine.

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