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102451-68-3

2-(4-chlorophenyl)-3-(2-nitro-1-phenylethyl)-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102451-68-3 Structure

  • Basic information

    1. Product Name: 2-(4-chlorophenyl)-3-(2-nitro-1-phenylethyl)-1H-indole
    2. Synonyms: 2-(4-chlorophenyl)-3-(2-nitro-1-phenylethyl)-1H-indole
    3. CAS NO:102451-68-3
    4. Molecular Formula:
    5. Molecular Weight: 376.842
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102451-68-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(4-chlorophenyl)-3-(2-nitro-1-phenylethyl)-1H-indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-chlorophenyl)-3-(2-nitro-1-phenylethyl)-1H-indole(102451-68-3)
    11. EPA Substance Registry System: 2-(4-chlorophenyl)-3-(2-nitro-1-phenylethyl)-1H-indole(102451-68-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 102451-68-3(Hazardous Substances Data)

102451-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102451-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,5 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102451-68:
(8*1)+(7*0)+(6*2)+(5*4)+(4*5)+(3*1)+(2*6)+(1*8)=83
83 % 10 = 3
So 102451-68-3 is a valid CAS Registry Number.

102451-68-3Downstream Products

102451-68-3Relevant articles and documents

Microwave-accelerated Conjugate Addition of 2-Arylindoles to Substituted β-Nitrostyrenes in the Presence of Ammonium Trifluoroacetate: An Efficient Approach for the Synthesis of a Novel Class of CB1 Cannabinoid Receptor Allosteric Modulators

Kulkarni, Pushkar M.,Ranade, Ameya,Garai, Sumanta,Thakur, Ganesh A.

, p. 2079 - 2084 (2017)

2-Arylindoles, in general, exhibit reduced reactivity towards the conjugate addition to substituted nitrostyrenes, when compared with indoles. We report here an efficient, expeditious, and high-yielding conjugate addition of 2-arylindoles to substituted β

Synthesis of Spiro[indole-3,5′-isoxazoles] with Anticancer Activity via a Formal [4 + 1]-Spirocyclization of Nitroalkenes to Indoles

Aksenov, Alexander V.,Aksenov, Dmitrii A.,Arutiunov, Nikolai A.,Aksenov, Nicolai A.,Aleksandrova, Elena V.,Zhao, Zhenze,Du, Liqin,Kornienko, Alexander,Rubin, Michael

, p. 7123 - 7137 (2019/06/18)

An acid-assisted [4 + 1]-cycloaddition of indoles with nitrostyrenes affords 4′H-spiro[indole-3,5′-isoxazoles] in a diastereomerically pure form. Several of these spirocyclic molecules exhibit promising anticancer activity by reducing viability and inducing differentiation of neuroblastoma cells.

Allosteric modulators of CB1 cannabinoid receptors

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Page/Page column 27; 28; 31; 32, (2017/02/24)

The present invention relates to novel heterocyclic derivatives which are allosteric modulators of cannabinoid receptor 1 (CB1) and which are useful for the treatment or prevention of neurological and psychiatric disorders associated with endocannabinoid

ALLOSTERIC MODULATORS OF CB1 CANNABINOID RECEPTORS

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Paragraph 0083; 0106, (2013/07/19)

The present invention relates to novel heterocyclic derivatives which are allosteric modulators of cannabinoid receptor 1 (CB1) and which are useful for the treatment or prevention of neurological and psychiatric disorders associated with endocannabinoid

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