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40468-86-8

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40468-86-8 Usage

Synthesis Reference(s)

Chemical and Pharmaceutical Bulletin, 18, p. 511, 1970 DOI: 10.1248/cpb.18.511

Check Digit Verification of cas no

The CAS Registry Mumber 40468-86-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,6 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40468-86:
(7*4)+(6*0)+(5*4)+(4*6)+(3*8)+(2*8)+(1*6)=118
118 % 10 = 8
So 40468-86-8 is a valid CAS Registry Number.

40468-86-8 Well-known Company Product Price

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  • Aldrich

  • (695939)  trans-N-(2-Pyridylmethylene)aniline  97%

  • 40468-86-8

  • 695939-1G

  • 483.21CNY

  • Detail
  • Aldrich

  • (695939)  trans-N-(2-Pyridylmethylene)aniline  97%

  • 40468-86-8

  • 695939-5G

  • 1,251.90CNY

  • Detail

40468-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-N-Phenyl-1-(2-pyridinyl)methanimine

1.2 Other means of identification

Product number -
Other names N-(2-Pyridylmethylidene)aniline

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:40468-86-8 SDS

40468-86-8Relevant articles and documents

193. Photoformation of (Z)-Isomers in Diarylazomethines. Part IV. Direct and Sensitized Photoisomerization of Pyridyl Analogues of Benzylidene-aniline and Absorption Spectra of their (Z)-Isomers

Maeda, Koko,Fischer, Ernst

, p. 1961 - 1965 (1983)

UV irradiation of solutions of the (E)-isomers of five (out of the possible six) monopyridyl analogues at reduced temperatures results in extensive (80-90percent) conversion into the corresponding (Z)-isomers.The process is reversible both thermally and photochemically.The (Z)-isomers are stable at temperatures below -80 deg, and their absorption spectra were estimated.Biacetyl-photosensitized (E)->(Z) isomerization was observed, with (Z)-contents of ca. 70percent at the photostationary state.

Superelectrophilic Diels–Alder reactions and oxidations leading to heterocyclic biaryl compounds

Vuong, Hien,Klumpp, Douglas A.

supporting information, p. 316 - 323 (2019/01/18)

Heterocyclic imines provide biaryl products by a two-step transformation. The first transformation involves a Diels–Alder reaction with a multiply protonated imine to give a tetrahydroquinoline product, whereas the second step involves oxidation with elem

Diels-Alder Reactions with Ethylene and Superelectrophiles

Vuong, Hien,Dash, Barada P.,Nilsson Lill, Sten O.,Klumpp, Douglas A.

supporting information, p. 1849 - 1852 (2018/04/16)

Diels-Alder reactions have been accomplished with ethylene as the dienophile through the use of inverse-electron demand Diels-Alder chemistry. As a key aspect of the chemistry, the dienes are part of tri- or dicationic superelectrophilic systems. Theoreti

Silver(I)-pyridinyl Schiff base complexes: Synthesis, characterisation and antimicrobial studies

Njogu, Eric M.,Omondi, Bernard,Nyamori, Vincent O.

, p. 118 - 128 (2017/02/05)

Fifteen new silver(I)-pyridinyl complexes of the general formula [AgL2]X, where X = ClO4?, OTf or NO3?, were synthesised by reacting (E)-N-(pyridinylmethylene)aniline ligands and the respective silver

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