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Cyclohexanamine, N-(1H-pyrrol-2-ylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

274687-34-2

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274687-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 274687-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,4,6,8 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 274687-34:
(8*2)+(7*7)+(6*4)+(5*6)+(4*8)+(3*7)+(2*3)+(1*4)=182
182 % 10 = 2
So 274687-34-2 is a valid CAS Registry Number.

274687-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(pyrrol-2-ylidenemethyl)cyclohexanamine

1.2 Other means of identification

Product number -
Other names Cyclohexanamine,N-(1H-pyrrol-2-ylmethylene)

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:274687-34-2 SDS

274687-34-2Downstream Products

274687-34-2Relevant academic research and scientific papers

Violet-blue emitting 2-(N-alkylimino)pyrrolyl organoboranes: Synthesis, structure and luminescent properties

Krishnamoorthy, Paramasivam,Ferreira, Bruno,Gomes, Clara S.B.,Vila-Vi?osa, Diogo,Charas, Ana,Morgado, Jorge,Calhorda, Maria José,Ma?anita, António L.,Gomes, Pedro T.

, p. 520 - 532 (2017)

The condensation reactions of 2-formylpyrrole (1) or 2-formylphenanthro[9,10-c]pyrrole (2) with various aliphatic amines afforded the corresponding 2-iminopyrrole ligand precursors 3–10, which, upon stoichiometric reaction with BPh3, led to the

Living ethylene/norbornene copolymerisation catalyzed by titanium complexes having two pyrrolide-imine chelate ligands

Yoshida, Yasunori,Saito, Junji,Mitani, Makoto,Takagi, Yukihiro,Matsui, Shigekazu,Ishii, Sei-Ichi,Nakano, Takashi,Kashiwa, Norio,Fujita, Terunori

, p. 1298 - 1299 (2002)

Ethylene/norbornene copolymerisation behaviour of titanium complexes with two pyrrolide-imine chelate ligands is described.

Titanium complexes of pyrrolylaldiminate ligands and their exploitation for the ring-opening polymerization of cyclic esters

Chuawong, Pitak,Hormnirun, Pimpa,Nanok, Tanin,Upitak, Kanokon,Wattanathana, Worawat

, p. 10964 - 10981 (2021/08/17)

A series of six-coordinate titanium complexes1-6supported by pyrrolylaldiminate ligands were preparedviathe reaction of 2 equivalents of ligands and Ti(OiPr)4in toluene at 70 °C. The X-ray structure of2revealed that the two ligands w

Hydrogen-Bond Catalysis of Imine Exchange in Dynamic Covalent Systems

Schaufelberger, Fredrik,Seigel, Karolina,Ramstr?m, Olof

, p. 15581 - 15588 (2020/10/02)

The reversibility of imine bonds has been exploited to great effect in the field of dynamic covalent chemistry, with applications such as preparation of functional systems, dynamic materials, molecular machines, and covalent organic frameworks. However, acid catalysis is commonly needed for efficient equilibration of imine mixtures. Herein, it is demonstrated that hydrogen bond donors such as thioureas and squaramides can catalyze the equilibration of dynamic imine systems under unprecedentedly mild conditions. Catalysis occurs in a range of solvents and in the presence of many sensitive additives, showing moderate to good rate accelerations for both imine metathesis and transimination with amines, hydrazines, and hydroxylamines. Furthermore, the catalyst proved simple to immobilize, introducing both reusability and extended control of the equilibration process.

Synthesis, characterization and cancer cell growth inhibition activity of ruthenium(II) complexes bearing bidentate pyrrole-imine ligands

Chen, Guan-Hao,Leu, Wohn-Jenn,Guh, Jih-Hwa,Lin, Chia-Her,Huang, Jui-Hsien

, p. 122 - 130 (2018/05/28)

A series of bidentate pyrrole-imine ligands, [C4H3NH-(2-CH=N-R)] (1, R = cyclohexenyl; 2, R = CH2CH2-1-cyclohexenyl; 3, R = tBu; 4, R = CH2-2-furyl; 5, R = 2-methoxylphenyl; 6, R = phenyl;

PHOSPHORESCENT IRIDIUM COMPLEXES

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Paragraph 0052; 0053; 0054, (2016/10/17)

Metal complexes of formula I and IA and polymers derived from the complexes are useful in optoelectronic devices wherein M is Ir, Co or Rh; is a cyclometallated ligand; R1 is hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, or substi

Novel vanadium(iii) complexes with bidentate N,N-chelating iminopyrrolide ligands: Synthesis, characterization and catalytic behaviour of ethylene polymerization and copolymerization with 10-undecen-1-ol

Xu, Bao-Chang,Hu, Tao,Wu, Ji-Qian,Hu, Ning-Hai,Li, Yue-Sheng

body text, p. 8854 - 8863 (2010/02/16)

A series of novel vanadium(iii) complexes bearing iminopyrrolide chelating ligands [2-(RNCH)C4H3N]V(THF)2Cl2 (2a: R = cyclohexyl; 2b: R = Ph; 2c: R = 2,6-iPr2C6H 3; 2d: R = p-CF

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