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Oxidronic acid, also known as Oxidronic, is a synthetic derivative of the naturally occurring compound deoxycholic acid. It is a bile acid that has been used in medicine for various purposes, including the treatment of certain types of gallstones and as a component in some cholesterol-lowering medications. Oxidronic acid works by helping to dissolve cholesterol stones in the gallbladder, thus aiding in their removal. It is important to note that the use of Oxidronic acid should be under the supervision of a healthcare professional, as it can have side effects and may not be suitable for all individuals.

1546-10-7

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1546-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1546-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,4 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1546-10:
(6*1)+(5*5)+(4*4)+(3*6)+(2*1)+(1*0)=67
67 % 10 = 7
So 1546-10-7 is a valid CAS Registry Number.

1546-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohex-1-en-1-yl-3-fluorobenzene

1.2 Other means of identification

Product number -
Other names 1-Cyclohex-1-enyl-3-fluoro-benzene

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:1546-10-7 SDS

1546-10-7Downstream Products

1546-10-7Relevant academic research and scientific papers

Visible-Light Photoredox Catalyzed Dehydrogenative Synthesis of Allylic Carboxylates from Styrenes

Bandini, Marco,Battaglioli, Simone,Liu, Yang,Lombardi, Lorenzo,Menichetti, Arianna,Montalti, Marco,Valenti, Giovanni

supporting information, p. 4441 - 4446 (2021/06/28)

The visible-light photoredox/[Co(III)] cocatalyzed dehydrogenative functionalization of cyclic and acyclic styryl derivatives with carboxylic acids is documented. The methodology enables the chemo- and regioselective allylic functionalization of styryl compounds, leading to allylic carboxylates (32 examples) under stoichiometric acceptorless conditions. Intermolecular as well as intramolecular variants are documented in high yields (up to 82%). A mechanistic rationale is also proposed on the basis of a combined experimental and spectroscopic investigation.

Mechanistic switch via subtle ligand modulation: Palladium-catalyzed synthesis of α,β-substituted styrenes via C-H bond functionalization

Flores-Gaspar, Areli,Martin, Ruben

, p. 1223 - 1228 (2011/06/26)

A new catalyst system able to efficiently perform the synthesis of styrenes via C-H bond functionalization and a subtle ligand modification are described. The high level of activity achieved allows for the synthesis of highly functionalized α,β-substituted styrenes, even the elusive E-configured trisubstituted olefins, in a regio- and stereoselective manner. Mechanistic experiments allowed for the identification of the corresponding synthetic intermediates.

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