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Phenol, 2-[[(4,6-dimethyl-2-pyridinyl)imino]methyl]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90440-99-6

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90440-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90440-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,4 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90440-99:
(7*9)+(6*0)+(5*4)+(4*4)+(3*0)+(2*9)+(1*9)=126
126 % 10 = 6
So 90440-99-6 is a valid CAS Registry Number.

90440-99-6SDS

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 2-{[(E)-4,6-Dimethyl-pyridin-2-ylimino]-methyl}-phenol

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:90440-99-6 SDS

90440-99-6Relevant academic research and scientific papers

Phosphorus-nitrogen compounds: Synthesis and spectral investigations on new spiro-cyclic phosphazene derivatives

Dal, Hakan,Suezen, Yasemin

, p. 1392 - 1397 (2007)

The condensation reaction of {N-[(2-hydroxyphenylmethyl)amino]-4,6-dimethylpyridine} (2), which is a reduction product of 1, with trimer N3P3Cl6 affords partially a substituted spiro-cyclic phosphazene derivative (3). The

Ruthenium N-Heterocyclic Carbene Complexes for Chemoselective Reduction of Imines and Reductive Amination of Aldehydes and Ketones

Kathuria, Lakshay,Samuelson, Ashoka G.

supporting information, (2020/06/17)

Chemoselective reduction of imines to secondary amines is catalyzed efficiently by tethered and untethered, half-sandwich ruthenium N-heterocyclic carbene (NHC) complexes at room temperature. The untethered Ru-NHC complexes are more efficient as catalysts for the reduction of aldimines and ketimines than the tethered complexes. Using the best untethered complex as a catalyst, electronic and steric demands on the reaction was probed using a series of imines. Chemoselectivity of the catalyst towards imine reduction was tested by performing inter and intramolecular competitive reactions in a variety of ways. The catalyst exhibits a very high TON and TOF under anaerobic conditions.

Hydrogen Bonding and Tautomeric Equilibria in Schiff Bases Derived from 2-Aminopyridines: Electronic Spectral Evidence for Substituent Effects

Ranganathan, Hemalatha,Ramasami, T.,Ramaswamy, D.,Santappa, M.

, p. 127 - 130 (2007/10/02)

Schiff bases of the type C6H3(R)(OH)CH=NC5H3N(Y) have now been synthesised and evidence sought for th

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