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N-ethyl-N-((6-methylpyridin-2-yl)methyl)ethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

863971-65-7

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863971-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863971-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,9,7 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 863971-65:
(8*8)+(7*6)+(6*3)+(5*9)+(4*7)+(3*1)+(2*6)+(1*5)=217
217 % 10 = 7
So 863971-65-7 is a valid CAS Registry Number.

863971-65-7SDS

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 2-diethylaminomethyl-6-methylpyridine

1.2 Other means of identification

Product number -
Other names -

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:863971-65-7 SDS

863971-65-7Relevant academic research and scientific papers

Metal-free C(sp3)-H bond sulfonyloxylation of 2-alkylpyridines and alkylnitrones

Wang, Chang-Sheng,Dixneuf, Pierre H.,Soulé, Jean-Fran?ois

, p. 4954 - 4957 (2018/07/25)

Pyridin-2-ylmethyl tosylate derivatives are obtained in high yields from 2-alkylpyridine 1-oxides via a [3,3]-sigmatropic rearrangement of the adduct between 2-alkylpridine 1-oxides with benzenesulfonyl chlorides. Moreover, alkylnitrones also undergo [3,3]-sigmatropic rearrangement to give α-tosylated ketones after hydrolysis. Substitution reactions with nucleophiles then lead to diverse useful functionalizations for the synthesis of pincer ligands.

Facile conversion of alcohols into esters and dihydrogen catalyzed by new ruthenium complexes

Zhang, Jing,Leitus, Gregory,Ben-David, Yehoshoa,Milstein, David

, p. 10840 - 10841 (2007/10/03)

An efficient, environmentally benign method for the preparation of esters from alcohols under mild, neutral conditions without the need for carboxylic acid derivatives and condensing agents was developed. Catalyst design, based on new Ru(II) hydrido carbonyl complexes incorporating electron-rich PNP and PNN ligands has resulted in the novel complex (I) which is an outstanding catalyst for the dehydrogenation of primary alcohols to esters and H2 under neutral conditions. Copyright

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