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(rac)-N-([2.2]paracyclophane-4-ylmethylene)aniline is a complex organic compound characterized by its unique molecular structure. It features a [2.2]paracyclophane-4-ylmethylene group, which is a cyclic alkene with a specific arrangement of carbon atoms, connected to an aniline moiety through an imine linkage. Aniline is a derivative of benzene with an amino group attached to the ring. (rac)-N-([2.2]paracyclophane-4-ylmethylene)aniline is a racemic mixture, meaning it consists of equal amounts of both the R and S enantiomers, which are mirror images of each other. The compound is of interest in the field of organic chemistry, particularly in the study of chiral molecules and their properties. It may also have potential applications in the development of new materials or pharmaceuticals due to its specific structural features.

88072-30-4

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88072-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88072-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,7 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88072-30:
(7*8)+(6*8)+(5*0)+(4*7)+(3*2)+(2*3)+(1*0)=144
144 % 10 = 4
So 88072-30-4 is a valid CAS Registry Number.

88072-30-4Downstream Products

88072-30-4Relevant academic research and scientific papers

Novel multichiral diols and diamines by highly stereoselective pinacol coupling of planar chiral [2.2]paracyclophane derivatives

Sergeeva, Elena V.,Rozenberg, Valeria I.,Antonov, Dmitrii Yu.,Vorontsov, Evgenii V.,Starikova, Zoya A.,Fedyanin, Ivan V.,Hopf, Henning

, p. 6944 - 6961 (2007/10/03)

The TiCl4/Zn-mediated intermolecular pinacol coupling of the planar chiral carbonyl compounds [2.2]paracyclophane-4-carbaldehyde, 4-acetyl[2.2]paracyclophane (ketone) and the four regioisomeric 5-, 7-, 12- and 13-methoxy[2.2]paracyclophane-4-ca

First stereoselective pinacol coupling in the [2.2]paracyclophane series

Sergeeva, Elena V.,Rozenberg, Valeria I.,Antonov, Dmitrii Yu.,Vorontsov, Evgenii V.,Starikova, Zoya A.,Hopf, Henning

, p. 1121 - 1123 (2007/10/03)

The planar chiral N-arylimines of [2.2]paracyclophane undergo stereoselective pinacol coupling under the action of the Zn/Cu couple in the presence of p-TosOH, thus forming N-aryl substituted 1,2-diamines. The stereoselective formation of the asymmetric c

Synthesis and reactions of 4-formyl paracyclophane

ELtamany, Elsayed H

, p. 238 - 242 (2007/10/02)

Paracyclophane (I) may be formylated in one-step under Rieche reaction conditions to give aldehyde (II) which easily undergoes condensation with amines, hydrazines and hydroxylamine hydrochloride.It also condenses with some ketones under Claisen-Schm

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