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873056-45-2

4-(2-Aminophenyl)benzyl alcohol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 873056-45-2 Structure

  • Basic information

    1. Product Name: 4-(2-Aminophenyl)benzyl alcohol
    2. Synonyms: 4-(2-Aminophenyl)benzyl alcohol;4-(3-Aminophenyl)benzyl alcohol;[4-(2-aminophenyl)phenyl]methanol
    3. CAS NO:873056-45-2
    4. Molecular Formula: C13H13NO
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 873056-45-2.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-(2-Aminophenyl)benzyl alcohol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(2-Aminophenyl)benzyl alcohol(873056-45-2)
    11. EPA Substance Registry System: 4-(2-Aminophenyl)benzyl alcohol(873056-45-2)

  • 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: 873056-45-2(Hazardous Substances Data)

873056-45-2 Usage

General Description

4-(2-Aminophenyl)benzyl alcohol, also known as 2-APBA, is a chemical compound with the molecular formula C13H13NO. It is often used in the synthesis of various pharmaceuticals and organic compounds. 2-APBA has been studied for its potential use in the development of new drugs, particularly in the treatment of neurological disorders. It has also been used in research as a building block for the synthesis of various organic molecules. The compound is a white solid at room temperature and is soluble in organic solvents such as ethanol and acetone. Its chemical structure consists of a benzyl alcohol molecule with an aminophenyl group attached to the benzene ring, making it a versatile compound for various chemical reactions and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 873056-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,0,5 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 873056-45:
(8*8)+(7*7)+(6*3)+(5*0)+(4*5)+(3*6)+(2*4)+(1*5)=182
182 % 10 = 2
So 873056-45-2 is a valid CAS Registry Number.

873056-45-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(2-aminophenyl)phenyl]methanol

1.2 Other means of identification

Product number -
Other names [1,1'-Biphenyl]-4-methanol,2'-amino

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:873056-45-2 SDS

873056-45-2Downstream Products

873056-45-2Relevant articles and documents

Visible-light-promoted intramolecular C-H amination in aqueous solution: Synthesis of carbazoles

Yang, Lizheng,Zhang, Yipin,Zou, Xiaodong,Lu, Hongjian,Li, Guigen

, p. 1362 - 1366 (2018/03/26)

An effective and operationally simple protocol is reported for the synthesis of versatile carbazoles. With water as a co-solvent, visible-light rather than various metals is used to facilitate the conversion of readily available 2-azidobiphenyls under mild conditions. Various functionalized bioactive natural alkaloids, such as glycoborine, clausine C, clausine L, clausine H and clauszoline K, were synthesized efficiently with nitrogen as a sole byproduct. The reaction could be performed in water, acidic or alkaline buffer solutions, showing its potential for applications in biochemistry.

Palladium-Catalyzed Intramolecular C–H Amination in Water

Yang, Lizheng,Li, Hao,Zhang, Haifei,Lu, Hongjian

, p. 5611 - 5615 (2016/12/14)

Palladium(II) catalysis was found to be effective for intramolecular C–H amination in water. With 2-azidobiphenyls as substrates, the reaction efficiently provided various carbazoles with N2as the sole byproduct. The reaction showed high functional-group tolerance and could be used in the synthesis of several natural carbazole alkaloids. The catalytic process was promoted by water, and the reaction was inefficient in the organic solvents that were investigated.

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