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161106-42-9

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161106-42-9 Usage

Description

(4R)-4-Isobutyl-2-oxazolidinone, also known as Isoxsuprine, is a chemical compound belonging to the class of oxazolidinone compounds. It possesses potential pharmacological properties and is commonly used as a vasodilator to improve blood flow in certain medical conditions.

Uses

Used in Cardiovascular Medicine:
(4R)-4-Isobutyl-2-oxazolidinone is used as a vasodilator for improving blood flow in conditions such as peripheral vascular disease, arteriosclerosis, and Raynaud's disease. It works by relaxing and widening the blood vessels, which in turn increases blood flow to certain parts of the body.
Used in Obstetric Medicine:
(4R)-4-Isobutyl-2-oxazolidinone is used as a uterine relaxant in obstetric medicine to improve blood flow to the placenta in cases of preterm labor. This helps in reducing the risk of complications associated with preterm birth.
(4R)-4-Isobutyl-2-oxazolidinone has been found to be generally well-tolerated with minimal side effects when used as directed by a healthcare professional.

Check Digit Verification of cas no

The CAS Registry Mumber 161106-42-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,1,0 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 161106-42:
(8*1)+(7*6)+(6*1)+(5*1)+(4*0)+(3*6)+(2*4)+(1*2)=89
89 % 10 = 9
So 161106-42-9 is a valid CAS Registry Number.

161106-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-methylpropyl)-1,3-oxazolidin-2-one

1.2 Other means of identification

Product number -
Other names HMS2194K20

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:161106-42-9 SDS

161106-42-9Relevant articles and documents

Sequencing of Sequence-Defined Oligourethanes via Controlled Self-Immolation

Anslyn, Eric V.,Coronado, Jaime N.,Dahlhauser, Samuel D.,Escamilla, P. Rogelio,Glass, Samuel A.,Moor, Sarah R.,Rapagnani, Rachel M.,Saunders, Douglas P.,Shei, Jasper S.,Vandewalle, Abigail N.,York, Jordan T.

supporting information, p. 2744 - 2749 (2020/03/10)

Sequence-defined polymers show promise for biomimetics, self-assembly, catalysis, and information storage, wherein the primary structure begets complex chemical processes. Here we report the solution-phase and the high-yielding solid-phase syntheses of discrete oligourethanes and methods for their self-immolative sequencing, resulting in rapid and robust characterization of this class of oligomers and polymers, without the use of MS/MS. Crucial to the sequencing is the inherent reactivity of the terminal alcohol to "unzip" the oligomers, in a controlled and iterative fashion, releasing each monomer as a 2-oxazolidinone. By monitoring the self-immolation reaction via LC/MS, an applied algorithm rapidly produces the sequence of the oligourethane. Not only does this process provide characterization of structurally complex molecules, it works as a reader of molecular information.

N-Acylation of Oxazolidinones via Aerobic Oxidative NHC Catalysis

Ta, Linda,Axelsson, Anton,Sundén, Henrik

, p. 12261 - 12268 (2018/09/25)

The first N-acylation of synthetically useful oxazolidinones with aldehydes using aerobic oxidative NHC catalysis is reported. The reaction offers a broad scope of functionalized oxazolidinones in good to excellent yields. Careful choice of electron transfer mediators proved pivotal to achieve efficient aerobic N-acylation, which has previously proven difficult using NHC catalysis. The methodology allows a mild entry to acylated oxazolidinones, avoiding the use of hazardous and reactive prefunctionalized substrates.

Method of preparing oxazolidone

-

Paragraph 0027; 0028, (2017/02/09)

The invention discloses a method of preparing oxazolidone. The method uses aziridine and carbon dioxide as materials and imidazole ionic liquid modified Salen metal complex comprising polyether chains as a catalyst, and allows high-efficiency and high-selectivity catalytic synthesis of oxazolidone under a pressure of 0.1-2.0 Mpa at a temperature of 30-70 DEG C; the process has relatively mild reaction conditions, there is no need for any solvent or co-catalyst, and reaction time is short; in addition, the catalyst provided herein can form a homogeneous catalytic system with a substrate under certain temperature and pressure, and by adding the solvent, it is possible to separate from the reaction system to enable reuse.

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