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4167-73-1

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4167-73-1 Usage

Description

2-(3-HYDROXY-3-METHYLBUTYL)PHENOL, also known as HMBP, is a phenolic compound characterized by its molecular formula C11H16O2. It features a hydroxyl group and a methyl group attached to a butyl chain, which contribute to its versatile chemical properties. HMBP is recognized for its applications in various industries, including the production of antioxidants and UV stabilizers for polymers and plastics, as well as its role in the synthesis of pharmaceuticals and as a chemical intermediate in organic synthesis. Additionally, HMBP has demonstrated potential as an anti-inflammatory agent and is under investigation for its therapeutic effects in medical applications.

Uses

Used in Polymer and Plastics Industry:
2-(3-HYDROXY-3-METHYLBUTYL)PHENOL is used as an antioxidant and UV stabilizer for enhancing the durability and stability of polymers and plastics. Its presence helps protect materials from degradation caused by exposure to heat, light, and oxygen, thereby extending their service life and maintaining their physical properties.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2-(3-HYDROXY-3-METHYLBUTYL)PHENOL serves as a key chemical intermediate in the synthesis of various drugs. Its unique structure allows for the development of new pharmaceutical compounds with potential therapeutic benefits.
Used in Organic Synthesis:
2-(3-HYDROXY-3-METHYLBUTYL)PHENOL is utilized as a chemical intermediate in organic synthesis, enabling the creation of a wide range of organic compounds for various applications, from specialty chemicals to advanced materials.
Used in Anti-Inflammatory Applications:
HMBP has been studied for its potential as an anti-inflammatory agent, making it a candidate for use in medical applications where reducing inflammation is necessary for treatment or symptom management.
Used in Research and Development:
2-(3-HYDROXY-3-METHYLBUTYL)PHENOL is also used in research and development settings to explore its therapeutic effects and potential applications in various medical fields, including the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 4167-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,6 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4167-73:
(6*4)+(5*1)+(4*6)+(3*7)+(2*7)+(1*3)=91
91 % 10 = 1
So 4167-73-1 is a valid CAS Registry Number.

4167-73-1SDS

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-(3-hydroxy-3-methylbutyl)phenol

1.2 Other means of identification

Product number -
Other names -

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:4167-73-1 SDS

4167-73-1Relevant articles and documents

RAR-ALPHA COMPOUNDS FOR INFLAMMATORY DISEASE AND MALE CONTRACEPTION

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Paragraph 0107, (2021/06/26)

Modulators of retinoid acid receptor-alpha (RARα) of formula (I) are provided herein, as well as pharmaceutical compositions and methods relating thereto.

GPR120 RECEPTOR AGONISTS AND USES THEREOF

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Page/Page column 86, (2012/01/06)

GPR120 agonists are provided. These compounds are useful for the treatment of metabolic diseases, including Type II diabetes and diseases associated with poor glycemic control.

Addition of trialkylaluminum reagents to glyconolactones. Synthesis of 1-C-methyl GlcNAc oxazoline and thiazoline

Knapp, Spencer,Yang, Chunhua,Haimowitz, Thomas

, p. 7101 - 7104 (2007/10/03)

Addition of carbon nucleophiles to 2-acetamido-2-deoxygluconolactones fails for many reagents, but trialkylaluminums add alkyl smoothly. The product of methyl addition to 2-acetamido-2-deoxy-D-gluconolactone has been converted to 1-C-methyl GlcNAc thiazoline, a potential N-acetylhexosaminidase inhibitor, and to an O-protected 1-C-Me GlcNAc oxazoline, a potential 1-C-Me GlcNAc donor.

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