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22643-20-5

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22643-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22643-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,4 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22643-20:
(7*2)+(6*2)+(5*6)+(4*4)+(3*3)+(2*2)+(1*0)=85
85 % 10 = 5
So 22643-20-5 is a valid CAS Registry Number.

22643-20-5SDS

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 N-benzyl-N-octyloctan-1-amine

1.2 Other means of identification

Product number -
Other names N-Benzyl-N,N-dioctylamin

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:22643-20-5 SDS

22643-20-5Downstream Products

22643-20-5Relevant articles and documents

High-Throughput Screening of Reductive Amination Reactions Using Desorption Electrospray Ionization Mass Spectrometry

Cooks, R. Graham,Ferreira, Christina R.,Li, Yangjie,Logsdon, David L.,Paschoal Sobreira, Tiago Jose,Thompson, David H.

supporting information, p. 1647 - 1657 (2020/10/26)

This study describes the latest generation of a high-throughput screening system that is capable of screening thousands of organic reactions in a single day. This system combines a liquid handling robot with desorption electrospray ionization (DESI) mass spectrometry (MS) for a rapid reaction mixture preparation, accelerated synthesis, and automated MS analysis. A total of 3840 unique reductive amination reactions were screened to demonstrate the throughputs that are capable with the system. Products, byproducts, and intermediates were all monitored in full-scan mass spectra, generating a complete view of the reaction progress. Tandem mass spectrometry experiments were conducted to verify the identity of the products formed. The amine and electrophile reactivity trends represented in the data match what is expected from theory, indicating that the system accurately models the reaction performance. The DESI results correlated well with those generated using more traditional mass spectrometry techniques like liquid chromatography-mass spectrometry, validating the data generated by the system.

Tertiary amine synthesis method

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Paragraph 0052-0057, (2019/01/24)

The invention relates to the technical field of organic matters, and specifically relates to a tertiary amine synthesis method. Under the action of a catalyst, in the absence of solvent and alkali, primary amine, secondary amine, or a nitro derivative reacts with alcohol to prepare tertiary amine. The provided synthesis method has the advantages that no toxic solvent is used during the preparationprocess, the method is green and environmentally friendly, the atom utilization rate is high, the operation is simple, the application range of the functional groups and substrate is wide, and the yield of tertiary amine is high, in particular reactions between aliphatic amine and alcohol.

The invention provides a recyclable waste acid recovery extractant and its preparation method (by machine translation)

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Paragraph 0031; 0032; 0033; 0034; 0035; 0036; 0037; 0038, (2017/02/09)

The present invention provides a kind of recyclable waste acid recovery extractant and its preparation method, the molecular formula of the extractant is R1 R2 NR3 Tertiary amine, in the formula R1 , R2 Are the C8 - C10 straight chain alkane, R3 For the α - ethyl benzene or toluene. The extractant preparation method of alkyl halide, α - methyl benzylamine or benzylamine, catalyst and adding base in the solvent, after heating in backflow, evaporating the solvent, adding water and ethyl acetate extraction, after drying the organic phase is concentrated to get the product. The extractant with the aqueous solution of the present invention low wastage, small pollution to the environment, at the same time the recycling of acid, acid emission reduction, and reduction of environmental pollution. (by machine translation)

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