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3174-81-0

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3174-81-0 Usage

General Description

The chemical "4-phenyl-5,6-dihydro-2H-p" is a compound belonging to the class of phenyl compounds. It is a cyclic compound with a six-membered ring containing both carbon and hydrogen atoms. 4-phenyl-5,6-dihydro-2H-p... may have various applications in the field of organic chemistry and pharmacology due to its structure and potential properties. Its specific chemical and physical properties, as well as its potential uses, would depend on the exact structure and functional groups present in the molecule.

Check Digit Verification of cas no

The CAS Registry Mumber 3174-81-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3174-81:
(6*3)+(5*1)+(4*7)+(3*4)+(2*8)+(1*1)=80
80 % 10 = 0
So 3174-81-0 is a valid CAS Registry Number.

3174-81-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Phenyl-5,6-dihydro-2H-pyran

1.2 Other means of identification

Product number -
Other names 4-phenyl-3,6-dihydro-2H-pyran

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:3174-81-0 SDS

3174-81-0Relevant articles and documents

Continuous slurry plug flow Fe/ppm Pd nanoparticle-catalyzed Suzuki-Miyaura couplings in water utilizing novel solid handling equipment

Chang, Jim,Gallou, Fabrice,Lipshutz, Bruce H.,Plummer, Scott,Robinson, Richard I.,Smith, Marie,Wood, Alex B.

supporting information, p. 7724 - 7730 (2021/10/12)

Herein are reported initial efforts to develop a generally accessible flow process, applying a heterogenous nanocatalyst to aqueous micelle-enabled Suzuki-Miyaura coupling reactions. Also disclosed is a new engineering solution (i.e., a self-draining back pressure regulator), which, when applied, enabled 1.5 hours of continuous operation leading to the production of 20 grams of a pharmaceutical intermediate.

Photocatalyzed Transition-Metal-Free Oxidative Cross-Coupling Reactions of Tetraorganoborates**

Music, Arif,Baumann, Andreas N.,Boser, Florian,Müller, Nicolas,Matz, Florian,Jagau, Thomas C.,Didier, Dorian

supporting information, p. 4322 - 4326 (2021/02/11)

Readily accessible tetraorganoborate salts undergo selective coupling reactions under blue light irradiation in the presence of catalytic amounts of transition-metal-free acridinium photocatalysts to furnish unsymmetrical biaryls, heterobiaryls and arylated olefins. This represents an interesting conceptual approach to forge C?C bonds between aryl, heteroaryl and alkenyl groups under smooth photochemical conditions. Computational studies were conducted to investigate the mechanism of the transformation.

Electro-Olefination—A Catalyst Free Stereoconvergent Strategy for the Functionalization of Alkenes

Baumann, Andreas N.,Dechent, Jonas,Didier, Dorian,Jagau, Thomas C.,Müller, Nicolas,Music, Arif

supporting information, (2020/07/04)

Conventional methods carrying out C(sp2)?C(sp2) bond formations are typically mediated by transition-metal-based catalysts. Herein, we conceptualize a complementary avenue to access such bonds by exploiting the potential of electrochemistry in combination with organoboron chemistry. We demonstrate a transition metal catalyst-free electrocoupling between (hetero)aryls and alkenes through readily available alkenyl-tri(hetero)aryl borate salts (ATBs) in a stereoconvergent fashion. This unprecedented transformation was investigated theoretically and experimentally and led to a library of functionalized alkenes. The concept was then carried further and applied to the synthesis of the natural product pinosylvin and the derivatization of the steroidal dehydroepiandrosterone (DHEA) scaffold.

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