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(E)-Methyl4-(2-iodovinyl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 257294-28-3 Structure
  • Basic information

    1. Product Name: (E)-Methyl4-(2-iodovinyl)benzoate
    2. Synonyms: (E)-Methyl4-(2-iodovinyl)benzoate
    3. CAS NO:257294-28-3
    4. Molecular Formula: C10H9IO2
    5. Molecular Weight: 288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 257294-28-3.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: (E)-Methyl4-(2-iodovinyl)benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-Methyl4-(2-iodovinyl)benzoate(257294-28-3)
    11. EPA Substance Registry System: (E)-Methyl4-(2-iodovinyl)benzoate(257294-28-3)
  • 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: 257294-28-3(Hazardous Substances Data)

257294-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 257294-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,7,2,9 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 257294-28:
(8*2)+(7*5)+(6*7)+(5*2)+(4*9)+(3*4)+(2*2)+(1*8)=163
163 % 10 = 3
So 257294-28-3 is a valid CAS Registry Number.

257294-28-3Relevant articles and documents

Gold (I/III)-Catalyzed Trifluoromethylthiolation and Trifluoromethylselenolation of Organohalides

Mudshinge, Sagar R.,Yang, Yuhao,Xu, Bo,Hammond, Gerald B.,Lu, Zhichao

supporting information, (2022/02/10)

The first C?SCF3/SeCF3 cross-coupling reactions using gold redox catalysis [(MeDalphos)AuCl], AgSCF3 or Me4NSeCF3, and organohalides as substrates are reported. The new methodology enables a one-stop shop synthesis of aryl/alkenyl/alkynyl trifluoromethylthio- and selenoethers with a broad substrate scope (>60 examples with up to 97 % isolated yield). The method is scalable, and its robustness is evidenced by the late-stage functionalization of various bioactive molecules, which makes this reaction an attractive alternative in the synthesis of trifluoromethylthio- and selenoethers for pharmaceutical and agrochemical research and development.

ANTIBACTERIAL AGENTS

-

Page/Page column 124-125, (2009/01/24)

Antibacterial compounds of formula (I) are provided, as well as stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof; pharmaceutical compositions comprising such compounds; methods of treating bacterial infections by the administration of such compounds; and processes for the preparation of such compounds.

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