What is the Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)-?

Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)- is , while it's Molecular Formula is C15H9BrClNO. Used in Pharmaceutical Research and Development: Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)is utilized as a compound of interest in pharmaceutical research and development. Its unique structure and potential biological activity make it a candidate for the discovery of new therapeutic agents. The specific applications and efficacy of this compound in drug development would require in-depth investigation and clinical trials to determine its suitability and safety. Used in Chemical Research: In the field of chemical research, Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)serves as a subject for studying the effects of different substituents on the properties and reactivity of organic molecules. Understanding these effects can contribute to the advancement of organic chemistry and the design of new compounds with tailored properties for various applications.

What is the CAS number for Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)-?

The CAS number of Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)- is 91714-51-1.

What is Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)- (91714-51-1) used for?

Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)-, is an organic compound characterized by a complex chemical structure. It is a ketone with a carbonyl group that is bonded to both a phenyl ring and an indole ring. The presence of bromine and chlorine substituents on the molecule adds to its unique structural features. Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)may hold potential in research and pharmaceutical development due to its distinctive attributes and possible biological activities, which necessitate further exploration and analysis.

What is the Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)-?

Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)- is , while it's Molecular Formula is C15H9BrClNO. Used in Pharmaceutical Research and Development: Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)is utilized as a compound of interest in pharmaceutical research and development. Its unique structure and potential biological activity make it a candidate for the discovery of new therapeutic agents. The specific applications and efficacy of this compound in drug development would require in-depth investigation and clinical trials to determine its suitability and safety. Used in Chemical Research: In the field of chemical research, Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)serves as a subject for studying the effects of different substituents on the properties and reactivity of organic molecules. Understanding these effects can contribute to the advancement of organic chemistry and the design of new compounds with tailored properties for various applications.

What is the CAS number for Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)-?

The CAS number of Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)- is 91714-51-1.

What is Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)- (91714-51-1) used for?

Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)-, is an organic compound characterized by a complex chemical structure. It is a ketone with a carbonyl group that is bonded to both a phenyl ring and an indole ring. The presence of bromine and chlorine substituents on the molecule adds to its unique structural features. Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)may hold potential in research and pharmaceutical development due to its distinctive attributes and possible biological activities, which necessitate further exploration and analysis.

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91714-51-1

Product Name：3-chloro-7-(4-bromobenzoyl)-indole
Molecular Formula：C15H9BrClNO
Purity：99%
Molecular Weight：334.6

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Product Details;

CasNo： 91714-51-1

Molecular Formula： C15H9BrClNO

Reputable supplier selling 3-chloro-7-(4-bromobenzoyl)-indole 91714-51-1 with stock

Molecular Formula:C15H9BrClNO
Molecular Weight:334.6

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91714-51-1 Process route

: 91714-50-0
7-(4-bromobenzoyl)-1-hydro-indole

: 91714-51-1
(4-Bromo-phenyl)-(3-chloro-1H-indol-7-yl)-methanone

Conditions

Conditions	Yield
With N-chloro-succinimide; In dichloromethane; Ambient temperature;	64%
With N-chloro-succinimide; In N,N-dimethyl-formamide; at 30 ℃; for 1h;

: 496-15-1
1-indoline

: 91714-51-1
(4-Bromo-phenyl)-(3-chloro-1H-indol-7-yl)-methanone

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 1.) BCl₃, AlCl₃, 2.) aq. HCl / 1.) toluene, reflux, 20 h, 2.) toluene, reflux, 2.5 h 2: 85 percent / MnO₂ / CH₂Cl₂ / Heating 3: 64 percent / N-chlorosuccinimide / CH₂Cl₂ / Ambient temperature With hydrogenchloride; manganese(IV) oxide; N-chloro-succinimide; aluminium trichloride; boron trichloride; In dichloromethane;

91714-51-1 Upstream products

91714-50-0
7-(4-bromobenzoyl)-1-hydro-indole
496-15-1
1-indoline
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4-bromobenzenecarbonitrile
91714-41-9
(4-bromophenyl)(2,3-dihydro-1H-indol-7-yl)methanone

91714-51-1 Downstream products

91713-91-6
7-(4-bromobenzoyl)-1,3-dihydro-2H-indol-2-one

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