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4-(4-BOC-aminophenyl)phenol is a synthetic chemical compound with a distinctive molecular structure, featuring a phenol group, an aminophenyl group, and a protective tert-Butyloxycarbonyl (BOC) group. 4-(4-BOC-aminophenyl)phenol is not naturally occurring but is crucial in various scientific fields, particularly in medicinal chemistry and drug development, due to its versatile properties that enable the creation of complex and beneficial substances.

848853-75-8

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848853-75-8 Usage

Uses

Used in Medicinal Chemistry:
4-(4-BOC-aminophenyl)phenol is used as a building block for the synthesis of pharmaceutical compounds, leveraging its unique molecular structure to create a variety of therapeutic agents. The BOC group plays a crucial role in protecting the amine group during chemical reactions, ensuring the integrity of the molecule and facilitating the development of new drugs.
Used in Drug Development:
In the pharmaceutical industry, 4-(4-BOC-aminophenyl)phenol is utilized as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs). 4-(4-BOC-aminophenyl)phenol's ability to be modified and functionalized allows researchers to design and optimize drug candidates with specific therapeutic properties, enhancing the efficacy and safety of new medications.
Used in Chemical Research:
4-(4-BOC-aminophenyl)phenol serves as a valuable research tool in the field of organic chemistry, enabling scientists to explore novel reaction pathways and mechanisms. Its unique structure allows for the investigation of various chemical transformations, providing insights into the reactivity and selectivity of different functional groups.
Used in Material Science:
4-(4-BOC-aminophenyl)phenol's structural properties also make it a candidate for the development of new materials with specific properties, such as conductivity, stability, or catalytic activity. Researchers can exploit the versatility of 4-(4-BOC-aminophenyl)phenol to create innovative materials for various applications, including sensors, catalysts, or advanced materials for energy storage and conversion.

Check Digit Verification of cas no

The CAS Registry Mumber 848853-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,8,5 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 848853-75:
(8*8)+(7*4)+(6*8)+(5*8)+(4*5)+(3*3)+(2*7)+(1*5)=228
228 % 10 = 8
So 848853-75-8 is a valid CAS Registry Number.

848853-75-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl (4'-hydroxy-[1,1'-biphenyl]-4-yl)carbamate

1.2 Other means of identification

Product number -
Other names 4-(4-BOC-AMINOPHENYL)PHENOL

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:848853-75-8 SDS

848853-75-8Downstream Products

848853-75-8Relevant academic research and scientific papers

FUSED PYRIMIDINE COMPOUNDS AS KCC2

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Page/Page column 40; 42-43, (2021/09/17)

The invention concerns compounds of Formula (I): (I) or pharmaceutically acceptable salts thereof, wherein R1, R2, R7 and ring A have any of the meanings hereinbefore defined in the description; process for their preparation; pharmaceutical compositions containing them and their use in treating KCC2 mediated diseases.

BIPHENYLOXY-ACIDS

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Page/Page column 62-63, (2008/06/13)

The present invention relates generally to substituted biphenyloxy acids (such as 4'-aryl-amido-biphenyl--4(3)-yloxy-acids and 4’-aryl-amidomethyl-biphenyl-4(3)-yloxy-acids) and methods of using them.

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