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(1E,3E)-4-(tetra-O-acetyl-D-arabino-tetritol-1-yl)-1-phenyl-1,2-diaza-1,3-butadiene is a complex organic compound characterized by a 1,2-diaza-1,3-butadiene backbone, which features a phenyl group attached to the nitrogen atom. The molecule also contains a tetra-O-acetyl-D-arabino-tetritol moiety, which is a derivative of D-arabino-tetritol with four acetyl groups attached to the hydroxyl groups. This structure contributes to the compound's overall complexity and potential reactivity. The compound's stereochemistry is defined by the E,E configuration at the 1 and 3 positions, indicating the trans arrangement of the double bonds. This specific arrangement of atoms and functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

7253-55-6

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7253-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7253-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7253-55:
(6*7)+(5*2)+(4*5)+(3*3)+(2*5)+(1*5)=96
96 % 10 = 6
So 7253-55-6 is a valid CAS Registry Number.

7253-55-6Relevant academic research and scientific papers

A Facile and Expeditious Entry to Acyclic Carbohydrate-Derived 1,2-Diazabutadienes

Avalos, Martin,Babiano, Reyes,Cintas, Pedro,Jimenez, Jose L.,Palacios, Juan C.,Sanchez, Juan B.

, p. 945 - 956 (2007/10/02)

Chiral 1,2-diaza-1,3-butadienes derived from acyclic monosaccharides are easily prepared from the corresponding and readily available unprotected sugars in a two-step sequence.

DIASTEREOFACIAL SELECTIVITY IN DIELS-ALDER REACTIONS OF CHIRAL 1,2-DIAZA-1,3-BUTADIENES DERIVED FROM CARBOHYDRATES

Avalos, M.,Babiano, R.,Cintas, P.,Jimenez, J. L.,Molina, M. M.,et al.

, p. 2513 - 2516 (2007/10/02)

The synthesis of several 1,2-diaza-1,3-butadienes 1 derived from carbohydrates is described.The reaction of 1, as chiral dienophiles, with 1,4-benzoquinone, 1,4-naphthoquinone, and diethyl azodicarboxylate occurs with high ?-facial stereoselectivity.

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