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"R-1,T-3-dinitro-c-2,T-4-diphenylcyclobutane" is a complex organic compound with a unique molecular structure. It consists of a cyclobutane ring, which is a four-carbon cyclic structure, with two phenyl groups (C6H5) attached to the second and fourth carbon atoms. The compound is further characterized by the presence of two nitro groups (-NO2), which are attached to the first and third carbon atoms in a trans configuration. This specific arrangement of functional groups and the cyclobutane ring gives the compound distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science. The stereochemistry of the compound, indicated by the R and T prefixes, refers to the spatial arrangement of the atoms around the chiral centers, which can influence its reactivity and biological activity.

3698-78-0

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3698-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3698-78-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3698-78:
(6*3)+(5*6)+(4*9)+(3*8)+(2*7)+(1*8)=130
130 % 10 = 0
So 3698-78-0 is a valid CAS Registry Number.

3698-78-0Upstream product

3698-78-0Relevant academic research and scientific papers

Solid State Dimerisation of β-Nitrostyrene: a Disordered Photoreactive Crystal

Desiraju, Gautam R.,Pedireddi, V. R.

, p. 1112 - 1113 (1989)

The unusual solid state dimerisation of β-nitrostyrene to yield two isomeric cyclobutanes is accounted for by its disordered, photoreactive crystal structure which permits a trans--->cis isomerisation.

Crystal Engineering and Solid State Chemistry of some β-Nitrostyrenes

Pedireddi, V. Rao,Sarma, Jagarlapudi A. R. P.,Desiraju, Gautam R.

, p. 311 - 320 (2007/10/02)

The unusual solid state photodimerisation of (E)-β-nitrostyrene to yield 'topochemical' and 'nontopochemical' cyclobutanes is accounted for by its disordered, photoreactive crystal structure which is monoclinic, P21/c, Z = 4, a = 8.097(6) Angst

On the Chemistry of Acetylenic Titanium Compounds

Krause, Norbert,Seebach, Dieter

, p. 1845 - 1852 (2007/10/02)

Solutions of acetylenic titanium compounds of the type R-CC-Ti(OiPr)3 (5) were prepared in the usual way, and their reactions with various electrophiles were studied.The addition to aldehydes takes place at low temperature; however, for ketones, long reaction times at 0 deg C are necessary.Therefore a complete differentiation between these two functional groups can be achieved.In contrast to alkyl titanium compounds, the alkinyl derivatives are more basic than the corresponding lithium compounds.The use of reagents 5 instead of lithium acetylides does not result in a striking improvement of the diastereoselectivity of addition to chiral aldehydes.The phenyl-substituted reagent (5, R = C6H5) reacts with styrene oxide 25 at the higher substituted carbon atom selectively with 59percent retention.

CHEMICAL TRANSFORMATIONS OF UNSATURATED NITRO COMPOUNDS IN THE EXCITED STATE

Slavcheva, Yu. M.,Perekalin, V. V.,Lipina, E. S.,Pavlova, Z. F.

, p. 2067 - 2070 (2007/10/02)

As a result of γ-irradiation of 1,2-dinitrostyrene the following dimerization products were obtained: Isomeric 1,4-dinitro-2,3-diphenyl-1,3-butadienes, 1,4-dinitro-1,4-diphenyl-1,3-butadiene, and 1,2-dinitro-3,4-diphenyl-3-cyclobutene.Under γ-irradiation

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