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5650-41-9

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5650-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5650-41-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5650-41:
(6*5)+(5*6)+(4*5)+(3*0)+(2*4)+(1*1)=89
89 % 10 = 9
So 5650-41-9 is a valid CAS Registry Number.

5650-41-9SDS

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 3-hydroxy-1-phenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 3-Hydroxypropiophenone

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:5650-41-9 SDS

5650-41-9Relevant articles and documents

Catalytic Net Oxidative C-C Activation and Silylation of Cyclopropanols with a Traceless Acetal Directing Group

Avullala, Thirupataiah,Nguyen, Hiep H.,Dakarapu, Udaya Sree,Asgari, Parham,Hua, Yuanda,Jeon, Junha

, p. 1764 - 1774 (2022/02/07)

Redox-neutral carbon-carbon (C-C) bond activation and functionalization strategies of cyclopropanols that give metallo homoenolate have offered merits to construct a range of useful β-functionalized ketones in an inverse-polarity fashion. Discovery and id

Chemoselective Electrochemical Oxidation of Secondary Alcohols Using a Recyclable Chloride-Based Mediator

Sommer, Florian,Kappe, C. Oliver,Cantillo, David

supporting information, p. 166 - 170 (2021/06/16)

Selective anodic oxidation of alcohols in the presence of other functional groups can be accomplished by using nitroxyl radical mediators. However, the electrochemical chemoselective oxidation of secondary alcohols in the presence of primary alcohols is a

LIGHT INDUCED CATALYTIC C-H OXYGENATION OF ALKANES

-

Paragraph 00219-00220 00223; 00225, (2021/04/02)

A method of oxygenating a benzylic C-H bond is provided. The method comprises light induced activation of an initiator and subsequent reaction with oxygen, resulting in the formation of free radicals. Subsequently, free radicals catalyze the reaction of the benzylic C-H bond with oxygen, thereby forming an oxygenated compound.

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