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1,2-Ethanediamine, N,N'-dimethyl-N,N'-bis(2-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65838-16-6

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65838-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65838-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,3 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65838-16:
(7*6)+(6*5)+(5*8)+(4*3)+(3*8)+(2*1)+(1*6)=156
156 % 10 = 6
So 65838-16-6 is a valid CAS Registry Number.

65838-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-dimethyl-N,N'-bis(2-phenylethyl)ethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names 1,2-Ethanediamine,N,N'-dimethyl-N,N'-bis(2-phenylethyl)

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:65838-16-6 SDS

65838-16-6Downstream Products

65838-16-6Relevant academic research and scientific papers

Iron-Catalyzed Synthesis of 2-Aminofurans from 2-Haloketones and Tertiary Amines or Enamines

Wang, Le-Cheng,Geng, Hui-Qing,Peng, Jin-Bao,Wu, Xiao-Feng

, p. 2605 - 2616 (2020/04/24)

The selective synthesis of heterocycles from readily available substrates and catalyzed by an abundant and environmental benign catalyst continues to be an attractive topic. In this communication, we report an interesting protocol for the synthesis of 2-aminofurans. Starting from 2-haloketones and tertiary amines, with abundant iron salt as the catalyst, various 2-aminofurans were produced in good yields. Control experiments were performed to understand the reaction pathway. Based on the identified reaction pathway, the substrates for this transformation can be extended from tertiary amines to enamines and even with better final yields. Finally, a formal three-component reaction can also be realized by forming the enamines in-situ from aldehydes and amines.

Copper diamine complexes and their use as bleach activating catalysts

-

Page/Page column 7, (2008/06/13)

Bleach activators are herein disclosed having the stoichiometric formula: wherein R1, R2, R3, R4, R5 and R6 are each a radical selected from the group consisting of hydrogen, alkyl, aryl, alkylaryl, arylalkyl, phenyl, benzyl and mixtures thereof, or R5 and R6 together form a hydrogen carbon ring, n is an integer from 0 to 1, m is an integer from 1 to 2, and X is selected from mono- and polyvalent anions. These bleach activators are combined with a peroxygen compound capable of releasing hydrogen perioxide in an aqueous solution. The combination is especially effective in the removal of hydrophobic stains from fabrics.

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