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Benzene, 1,5-dichloro-3-iodo-2-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 60633-27-4 Structure
  • Basic information

    1. Product Name: Benzene, 1,5-dichloro-3-iodo-2-methoxy-
    2. Synonyms:
    3. CAS NO:60633-27-4
    4. Molecular Formula: C7H5Cl2IO
    5. Molecular Weight: 302.927
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 60633-27-4.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: Benzene, 1,5-dichloro-3-iodo-2-methoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1,5-dichloro-3-iodo-2-methoxy-(60633-27-4)
    11. EPA Substance Registry System: Benzene, 1,5-dichloro-3-iodo-2-methoxy-(60633-27-4)
  • 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: 60633-27-4(Hazardous Substances Data)

60633-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60633-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,3 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60633-27:
(7*6)+(6*0)+(5*6)+(4*3)+(3*3)+(2*2)+(1*7)=104
104 % 10 = 4
So 60633-27-4 is a valid CAS Registry Number.

60633-27-4Downstream Products

60633-27-4Relevant articles and documents

NOVEL THYROMIMETICS

-

, (2021/06/04)

Compounds are provided having the structure of Formula (I) or a pharmaceutically acceptable isomer, racemate, hydrate, solvate, isotope, or salt thereof, wherein R1, R2, X1, X2, Y1, and Y2 are as defined herein. Such compounds function as thyromimetics and have utility for treating diseases such as neurodegenerative disorders and fibrotic diseases. Pharmaceutical compositions containing such compounds are also provided, as are methods of their use and preparation.

Preparation method of pyrrole derivative and intermediate thereof

-

, (2021/10/27)

The invention discloses a preparation method of a pyrrole derivative and an intermediate thereof. , 2, 4 -dichlorophenol and 4 -bromo - 1H - pyrrole -2 - formaldehyde which are wide in source are used as raw materials and are substituted. The target compo

As neuroprotective agents of pharmaceutical compounds

-

, (2019/06/26)

The invention discloses a medicinal compound as a neuroprotective agent. The medicinal compound is a neuronal nitric oxide synthase-postsynaptic density protein 95 (nNOS-PSD95) decoupling agent. The medicinal compound is a benzene ring derivative shown in the general formula (I) or its pharmaceutically acceptable salt. The invention further discloses a preparation method of the medicinal compound and a use of the medicinal compound in prevention and treatment on neuronal damage influence-caused diseases.

Mesoionic pyrido[1,2-a]pyrimidinones: Discovery of dicloromezotiaz as a lepidoptera insecticide acting on nicotinic acetylcholine receptors1,2

Zhang, Wenming,Holyoke, Caleb W.,Barry, James,Cordova, Daniel,Leighty, Robert M.,Tong, My-Hanh T.,Hughes, Kenneth A.,Lahm, George P.,Pahutski, Thomas F.,Xu, Ming,Briddell, Twyla A.,McCann, Stephen F.,Henry, Yewande T.,Chen, Yuzhong

, p. 911 - 917 (2017/02/10)

A novel class of mesoionic pyrido[1,2-a]pyrimidinones has been discovered with exceptional insecticidal activity controlling a number of insect species. In this communication, we report the part of the optimization program that led to the identification o

Efficient and reliable iodination and o-Methylation of fluorinated phenols

Francke, Robert,Schnakenburg, Gregor,Waldvogel, Siegfried R.

experimental part, p. 2357 - 2362 (2010/07/04)

Fluorinated phenols and other electron-deficient phenolic substrates are efficiently and cleanly iodinated by an iodine/ iodide mixture employing alkaline conditions. This protocol turned out to be the most practical for the generation of such highly fluorinated iodophenols. For later application in coupling processes the protection of the phenolic hydroxy moiety is often required. Therefore, a practical iodination and subsequent methylation sequence was elaborated providing the highly fluorinated anisoles with good to excellent yields. The developed method is applicable for a broad scope of fluorinated phenols and analogues.

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