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(2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL, also known as 3-Hydroxy-2-(2-hydroxyphenyl)-5-methylbenzenamine, is a phenolic compound with a molecular formula C13H13NO2. It features an amine and hydroxyl functional group attached to a benzene ring, making it a versatile building block in organic synthesis and pharmaceutical research.

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  • 156261-32-4 Structure
  • Basic information

    1. Product Name: (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL
    2. Synonyms: (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL
    3. CAS NO:156261-32-4
    4. Molecular Formula: C14H15NO
    5. Molecular Weight: 213.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156261-32-4.mol
  • Chemical Properties

    1. Melting Point: 107 °C(Solv: ethanol (64-17-5))
    2. Boiling Point: 396.1±37.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.148±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 13.67±0.20(Predicted)
    10. CAS DataBase Reference: (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL(CAS DataBase Reference)
    11. NIST Chemistry Reference: (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL(156261-32-4)
    12. EPA Substance Registry System: (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL(156261-32-4)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 156261-32-4(Hazardous Substances Data)

156261-32-4 Usage

Uses

Used in Organic Synthesis:
(2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL is used as a building block for the synthesis of various bioactive molecules, contributing to the development of new compounds with potential applications across different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL serves as a key intermediate in the development of pharmaceuticals. Its unique structure allows for the creation of novel drugs with potential therapeutic effects.
Used in Medicinal Chemistry:
(2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL is utilized in medicinal chemistry for the exploration of its potential interactions with biological targets, which may lead to the discovery of new drugs and treatments.
Used in Drug Development:
As a component in drug development, (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL plays a crucial role in the formulation and optimization of new pharmaceutical agents, enhancing their efficacy and safety.
Safety Note:
It is important to handle (2-AMINO-5-METHYL-PHENYL)-PHENYL-METHANOL with care and follow proper safety guidelines to minimize health and environmental risks associated with this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 156261-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,2,6 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 156261-32:
(8*1)+(7*5)+(6*6)+(5*2)+(4*6)+(3*1)+(2*3)+(1*2)=124
124 % 10 = 4
So 156261-32-4 is a valid CAS Registry Number.

156261-32-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-amino-5-methylphenyl)-phenylmethanol

1.2 Other means of identification

Product number -
Other names 2-Amino-5-methyl-benzhydrol

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:156261-32-4 SDS

156261-32-4Relevant articles and documents

An efficient iron-promoted synthesis of 6H-indolo[2,3- b] quinolines and neocryptolepine derivatives

Yan, Zicong,Wan, Changfeng,Wan, Jianyong,Wang, Zhiyong

supporting information, p. 4405 - 4408 (2016/06/06)

A facile and practical method for the preparation of 6H-indolo[2,3-b]quinolines and neocryptolepines was developed under the promotion of the easily available ferric trichloride, affording the desired products with moderate to good yields.

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