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3-methylphenyl 2-iodobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 723259-87-8 Structure
  • Basic information

    1. Product Name: 3-methylphenyl 2-iodobenzoate
    2. Synonyms: 3-methylphenyl 2-iodobenzoate
    3. CAS NO:723259-87-8
    4. Molecular Formula: C14H11IO2
    5. Molecular Weight: 338.14041
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 723259-87-8.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: 3-methylphenyl 2-iodobenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-methylphenyl 2-iodobenzoate(723259-87-8)
    11. EPA Substance Registry System: 3-methylphenyl 2-iodobenzoate(723259-87-8)
  • 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: 723259-87-8(Hazardous Substances Data)

723259-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 723259-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,3,2,5 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 723259-87:
(8*7)+(7*2)+(6*3)+(5*2)+(4*5)+(3*9)+(2*8)+(1*7)=168
168 % 10 = 8
So 723259-87-8 is a valid CAS Registry Number.

723259-87-8Downstream Products

723259-87-8Relevant articles and documents

[N,P]-pyrrole PdCl2 complexes catalyzed the formation of dibenzo-α-pyrone and lactam analogues

Suárez-Meneses,Oukhrib,Gouygou,Urrutigo?ty,Daran,Cordero-Vargas,Ortega-Alfaro,López-Cortés

supporting information, p. 9621 - 9630 (2016/07/06)

We herein report the synthesis and catalytic application of a new family of [N,P] ligands based on the pyrrole ring with alpha-phosphine or phosphole units. Their palladium complexes (3a-d) were obtained in very good yields and their catalytic properties were evaluated in the direct intramolecular arylation to obtain both benzopyranones and phenanthridinones. The air stable complex 3a exhibited the best catalytic performance of this series of complexes, using 1 mol% of catalyst in combination with microwaves to promote this reaction.

Regioselectivity of the intramolecular biaryl coupling reaction of 3-substituted phenyl 2-iodobenzoate using a palladium reagent

Maeda, Kazuhiro,Matsukihira, Takuya,Saga, Shumpei,Takeuchi, Yasuo,Harayama, Takashi,Horino, Yoshikazu,Abe, Hitoshi

, p. 621 - 628 (2016/11/07)

This study investigated the regioselectivity of the intramolecular biaryl coupling reaction of the phenyl benzoate derivative which possesses a methyl or methoxy group at the meta-position of the phenoxy moiety. The type of base and the presence/absence of the phosphine ligand influenced the product ratio. A transition state model and the regioselectivity of the reaction are discussed.

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