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2-(2-amino-4-bromo-phenyl)-ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 856839-67-3 Structure
  • Basic information

    1. Product Name: 2-(2-amino-4-bromo-phenyl)-ethanol
    2. Synonyms: 2-(2-amino-4-bromo-phenyl)-ethanol
    3. CAS NO:856839-67-3
    4. Molecular Formula:
    5. Molecular Weight: 216.077
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 856839-67-3.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-(2-amino-4-bromo-phenyl)-ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-amino-4-bromo-phenyl)-ethanol(856839-67-3)
    11. EPA Substance Registry System: 2-(2-amino-4-bromo-phenyl)-ethanol(856839-67-3)
  • 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: 856839-67-3(Hazardous Substances Data)

856839-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 856839-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,8,3 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 856839-67:
(8*8)+(7*5)+(6*6)+(5*8)+(4*3)+(3*9)+(2*6)+(1*7)=233
233 % 10 = 3
So 856839-67-3 is a valid CAS Registry Number.

856839-67-3Relevant articles and documents

Enantioselective Copper-Catalyzed Intramolecular N?H Bond Insertion: Synthesis of Chiral 2-Carboxytetrahydroquinolines

Song, Xiao-Guang,Ren, Yuan-Yuan,Zhu, Shou-Fei,Zhou, Qi-Lin

, p. 2366 - 2370 (2016)

The first highly enantioselective intramolecular N?H bond insertion was realized by using copper catalysts modified with chiral spirobisoxazoline ligands, which provides a novel strategy for the synthesis of chiral 2-carboxytetrahydroquinolines. This reaction features fast reaction rate, high yield, high enantioselectivity, and mild reaction conditions. (Figure presented.).

AMINOBENZIMIDAZOLES AND BENZIMIDAZOLES AS INHIBITORS OF RESPIRATORY SYNCYTIAL VIRUS REPLICATION

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Page/Page column 41, (2008/06/13)

Aminobenzimidazoles and benzimidazoles having inhibitory activity on RSV replication and having the formula (I) the prodrugs, N-oxides, addition salts, quaternary amines, metal complexes and stereochemically isomeric forms thereof; wherein G is a direct b

MORPHOLINYL CONTAINING BENZIMIDAZOLES AS INHIBITORS OF RESPIRATORY SYNCYTIAL VIRUS REPLICATION

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Page/Page column 45, (2010/02/12)

The present invention concerns morpholinyl containing benzimidazoles having inhibitory activity on the replication of the respiratory syncytial virus and having the formula (I), a prodrug, N-oxide, addition salt, quaternary amine, metal complex or stereoc

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