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Pyridine, 3-butyl-2,4,6-triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105998-59-2

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105998-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105998-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,9 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105998-59:
(8*1)+(7*0)+(6*5)+(5*9)+(4*9)+(3*8)+(2*5)+(1*9)=162
162 % 10 = 2
So 105998-59-2 is a valid CAS Registry Number.

105998-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Butyl-2,4,6-triphenyl-pyridin

1.2 Other means of identification

Product number -
Other names 3-Butyl-2,4,6-triphenyl-pyridine

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:105998-59-2 SDS

105998-59-2Downstream Products

105998-59-2Relevant academic research and scientific papers

Highly functionalized pyridines synthesis from N-sulfonyl ketimines and alkynes using the N-S bond as an internal oxidant

Zhang, Qian-Ru,Huang, Ji-Rong,Zhang, Wei,Dong, Lin

, p. 1684 - 1687 (2014/04/17)

The N-S bond-based internal oxidant offers a distinct approach for the synthesis of highly functionalized pyridines. A novel Rh(III)-catalyzed one-pot process undergoes an efficient C-C/C-N bond formation along with desulfonylation under very mild conditions. The method is quite simple, general, and efficient.

Pyrylium Compounds. 30. C-Alkylation of 1,3,5-Triaryl-pentene-1,5-dione Enolates: A Simple Approach to 3-Alkylsubstituted 2,4,6-Triarylpyrylium Salts

Fischer, Gerhard W.

, p. 983 - 997 (2007/10/02)

1,3,5-Triaryl-pentene-1,5-dione enolates (10), obtainable in crystalline form from 2,4,6-triarylpyrylium pseudobases (9) and sodium methoxide in benzene/ether, react in dipolar aprotonic solvents (e.g.DMSO, DMF) with various types of alkyl iodides to give

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