Welcome to LookChem.com Sign In|Join Free
  • or
2-(4-Bromophenyl)-2-hydroxypropionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58244-32-9

Post Buying Request

58244-32-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

58244-32-9 Usage

Molecular Weight

414.26 g/mol

Appearance

White to off-white crystalline powder

Solubility

Practically insoluble in water, slightly soluble in ethanol, and soluble in acetic acid

Melting Point

243-249°C

Receptor Activity

Acts as a dopamine receptor agonist, specifically D2-like receptors (D2, D3, D4, and D5)

Primary Uses

Treatment of hyperprolactinemia, Parkinson's disease, and acromegaly

Mechanism of Action

Stimulates dopamine receptors in the brain to regulate hormone levels and improve symptoms associated with target conditions

Additional Research

Studied for potential anti-tumor effects and possible applications in the treatment of certain types of cancer

Therapeutic and Research Importance

Has diverse biological activities and significant implications in both treatment and research fields

Check Digit Verification of cas no

The CAS Registry Mumber 58244-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,4 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58244-32:
(7*5)+(6*8)+(5*2)+(4*4)+(3*4)+(2*3)+(1*2)=129
129 % 10 = 9
So 58244-32-9 is a valid CAS Registry Number.

58244-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Bromophenyl)-2-hydroxypropanoic acid

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:58244-32-9 SDS

58244-32-9Relevant academic research and scientific papers

Synthesis of α-hydroxycarboxylic acids from various aldehydes and ketones by direct electrocarboxylation: A facile, efficient and atom economy protocol

Singh, Kishanpal,Sohal, Harvinder Singh,Singh, Baljit

, p. 839 - 845 (2021/04/09)

In present work, the formation of α-hydroxycarboxylic acids have been described from various aromatic aldehydes and ketones via direct electrocarboxylation method with 80-92% of yield without any side product and can be purified by simple recrystallization using sacrificial Mg anode and Pt cathode in an undivided cell, CO2at (1 atm) was continuously bubbled in the cell throughout the reaction using tetrapropylammonium chloride as a supporting electrolyte in acetonitrile. The synthesized compounds obtained in fair to excellent yield with a high level of purity. The characterization of electrocarboxylated compounds was done with spectroscopic techniques like IR, NMR (1H & 13C), mass and elemental analysis.

NOVEL LXR MODULATORS WITH BICYCLIC CORE MOIETY

-

, (2020/01/24)

The present invention relates to bicyclic compounds (e.g. indoles) containing a sulfonyl moiety, which bind to the liver X receptor (LXRα and/or LΧΚβ) and act preferably as inverse agonists of LXR.

Stereospecific decarboxylative allylation of sulfones

Weaver, Jimmie D.,Ka, Being J.,Morris, David K.,Thompson, Ward,Tunge, Jon A.

supporting information; scheme or table, p. 12179 - 12181 (2010/10/03)

Allyl sulfonylacetic esters undergo highly stereospecific, palladium-catalyzed decarboxylative allylation. The reaction allows the stereospecific formation of tertiary homoallylic sulfones in high yield. In contrast to related reactions that proceed at -100 °C and require highly basic preformed organometallics, the decarboxylative coupling described herein occurs under mild nonbasic conditions and requires no stoichiometric additives. Allylation of the intermediate α-sulfonyl anion is more rapid than racemization, leading to a highly enantiospecific process. Density functional theory calculations indicate that the barrier for racemization is 9.9 kcal/mol, so the barrier for allylation must be 9.9 kcal/mol.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 58244-32-9