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1236162-19-8

4-Chloro-2-iodo-5-Methoxy-phenylaMine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1236162-19-8 Structure

  • Basic information

    1. Product Name: 4-Chloro-2-iodo-5-Methoxy-phenylaMine
    2. Synonyms: 4-Chloro-2-iodo-5-Methoxy-phenylaMine;4-CHLORO-2-IODO-5-METHOXYANILINE
    3. CAS NO:1236162-19-8
    4. Molecular Formula: C7H7ClINO
    5. Molecular Weight: 283.49405
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1236162-19-8.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: 4-Chloro-2-iodo-5-Methoxy-phenylaMine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Chloro-2-iodo-5-Methoxy-phenylaMine(1236162-19-8)
    11. EPA Substance Registry System: 4-Chloro-2-iodo-5-Methoxy-phenylaMine(1236162-19-8)

  • 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: 1236162-19-8(Hazardous Substances Data)

1236162-19-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1236162-19-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,1,6 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1236162-19:
(9*1)+(8*2)+(7*3)+(6*6)+(5*1)+(4*6)+(3*2)+(2*1)+(1*9)=128
128 % 10 = 8
So 1236162-19-8 is a valid CAS Registry Number.

1236162-19-8Upstream product

1236162-19-8Downstream Products

1236162-19-8Relevant articles and documents

Synthesis of 5-hydroxyquinolines

Li, Jianke,Kung, Daniel W.,Griffith, David A.

scheme or table, p. 3876 - 3878 (2010/08/19)

A series of 5-hydroxyquinolines has been prepared via the Skraup reaction. Several regioisomers were made either by selective displacement of a leaving group or by using a bromo substituent as a blocking group. The bromo group was found to be an excellent blocking group due to its stability during the Skraup reaction and easy removal thereafter. Halides at the 5-position of quinoline were found to be much more reactive than those at the 7- and 8-positions. Finally, we have also found a unique method to reduce the pyridyl ring on quinolines, leaving a halogen substituent untouched.

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