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2-methyl-3-(morpholin-4-yl)-1-phenylpropan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22386-00-1

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22386-00-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22386-00-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,8 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22386-00:
(7*2)+(6*2)+(5*3)+(4*8)+(3*6)+(2*0)+(1*0)=91
91 % 10 = 1
So 22386-00-1 is a valid CAS Registry Number.

22386-00-1SDS

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-methyl-3-morpholin-4-yl-1-phenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 2-Methyl-3-morpholino-1-phenyl-propan-1-on

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:22386-00-1 SDS

22386-00-1Relevant academic research and scientific papers

Visible Light Driven Copper(I) Catalyzed Oxyamination of Electron Deficient Alkenes?

Li, Sanliang,Chen, Qiaoyu,Li, Wenbo,Gu, Guangxin,Zhang, Junliang

, p. 1116 - 1122 (2020)

A visible light driven Cu(I)-catalyzed intermolecular oxyamination of electron-deficient olefins has been achieved by using O-benzoylhydroxylamines as donors both for amine and oxygen. The transformation properties afford mild conditions and a wide substrate scope, providing access to ester derivatives of β-amino alcohols with good yields and high regioselectivity.

Synthesis of Carbamates from Alkyl Bromides and Secondary Amines Using Silver Carbonate

Acharya, Vanitha,Mal, Sanjib,Kilaru, Jagadeesh P.,Montgomery, Mark G.,Deshpande, Sudhindra H.,Sonawane, Ravindra P.,Manjunath, Bhanu N.,Pal, Sitaram

supporting information, p. 378 - 387 (2020/01/22)

Synthesis of alkyl carbamates from alkyl bromides and secondary amines using silver carbonate as a carbonate source under mild condition is described. Various secondary amines and bromo derivatives were converted into alkyl carbamate derivatives in 33 to 62 % yield.

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