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1H-Indole, 3-(2-nitroethenyl)-2-phenyl- is a complex organic chemical compound with the molecular formula C16H12N2O2. It is a derivative of indole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to a pyrrole ring. The compound features a 2-phenyl group attached to the indole nucleus, and a 2-nitroethenyl group at the 3-position, which introduces a nitro group and a vinyl group to the molecule. This specific arrangement of functional groups endows the compound with unique chemical and physical properties, making it potentially useful in various applications, such as pharmaceuticals, agrochemicals, or materials science. However, due to the presence of a nitro group, it is essential to handle 1H-Indole, 3-(2-nitroethenyl)-2-phenyl- with caution, as nitro compounds can be sensitive to heat and friction, posing potential safety risks.

1225-93-0

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1225-93-0 Usage

Chemical class

Indole class of organic compounds

Structure

Nitrogen-containing five-membered ring

Substituents

2-nitroethenyl and phenyl groups

Potential uses

Chemical reactions, building block for synthesizing other organic compounds

Application fields

Chemistry, pharmaceuticals, and materials science

Handling precautions

Hazards and risks associated with its chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 1225-93-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1225-93:
(6*1)+(5*2)+(4*2)+(3*5)+(2*9)+(1*3)=60
60 % 10 = 0
So 1225-93-0 is a valid CAS Registry Number.

1225-93-0Relevant academic research and scientific papers

Identification of cb1 receptor allosteric sites using force-biased mmc simulated annealing and validation by structure-activity relationship studies

Hurst, Dow P.,Garai, Sumanta,Kulkarni, Pushkar M.,Schaffer, Peter C.,Reggio, Patricia H.,Thakur, Ganesh A.

supporting information, p. 1216 - 1221 (2019/08/27)

Positive allosteric modulation of the cannabinoid 1 receptor (CB1R) has demonstrated distinct therapeutic advantages that address several limitations associated with orthosteric agonism and has opened a promising therapeutic avenue for further drug development. To advance the development of CB1R positive allosteric modulators, it is important to understand the molecular architecture of CB1R allosteric site(s). The goal of this work was to use Force-Biased MMC Simulated Annealing to identify binding sites for GAT228 (R), a partial allosteric agonist, and GAT229 (S), a positive allosteric modulator (PAM) at the CB1R. Our studies suggest that GAT228 binds in an intracellular (IC) TMH1-2-4 exosite that would allow this compound to act as a CB1 allosteric agonist as well as a CB1 PAM. In contrast, GAT229 binds at the extracellular (EC) ends of TMH2/3, just beneath the EC1 loop. At this site, this compound can act as CB1 PAM only. Finally, these results were successfully validated through the synthesis and biochemical evaluation of a focused library of compounds.

An environmentally friendly protocol for oxidative halocyclization of tryptamine and tryptophol derivatives

Xu, Jun,Tong, Rongbiao

, p. 2952 - 2956 (2017/07/24)

An environmentally friendly and efficient protocol (KX/oxone) for oxidative halocyclization of tryptamine/tryptophol derivatives was developed and demonstrated with 28 examples and concise total synthesis of cyclotryptamine alkaloid protubonines A and B. The distinct advantage of this protocol over all previous methods is that no organic byproduct is generated from a halogenating agent or oxidant, thus greatly reducing the environmental impact of halocyclization and facilitating the post-reaction purification.

Asymmetric dearomatization of indoles through a Michael/Friedel-Crafts-Type cascade to construct polycyclic spiroindolines

Zhao, Xiaohu,Liu, Xiaohua,Mei, Hongjiang,Guo, Jing,Lin, Lili,Feng, Xiaoming

supporting information, p. 4032 - 4035 (2015/03/30)

A highly efficient asymmetric dearomatization of indoles was realized through a cascade reaction between 2-isocyanoethylindole and alkylidene malonates catalyzed by a chiral N,N-dioxide/MgII catalyst. Fused polycyclic indolines containing three stereocenters were afforded in good yields with excellent diastereo- and enantioselectivities through a Michael/Friedel-Crafts/Mannich cascade. When 2-substituted 2-isocyanoethylindoles were used, spiroindoline derivatives were obtained through a Michael/Friedel-Crafts reaction.

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