What is the 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)-?

1H-Benzimidazole, 5-chloro-2-(phenylmethyl)- is , while it's Molecular Formula is C14H11ClN2. Used in Pharmaceutical Research: 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)is utilized as a potential drug candidate in pharmaceutical research for its structural similarity to certain biologically active compounds, which may contribute to the development of new medications. Used in Medicinal Development: This chemical is employed as a precursor or building block in the synthesis of various therapeutic agents, potentially leading to the creation of antiviral, antibacterial, or antifungal medications. Used in Material Science: Given its unique chemical structure and potential reactivity, 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)may also find applications in material science, where its properties could be harnessed for specific material properties or functions. Used in Chemical Synthesis: 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)may serve as an intermediate or reactant in chemical synthesis processes, where its reactivity and structural features could be exploited to produce a range of other chemical products.

What is the CAS number for 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)-?

The CAS number of 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)- is 7118-63-0.

What is the 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)-?

1H-Benzimidazole, 5-chloro-2-(phenylmethyl)- is , while it's Molecular Formula is C14H11ClN2. Used in Pharmaceutical Research: 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)is utilized as a potential drug candidate in pharmaceutical research for its structural similarity to certain biologically active compounds, which may contribute to the development of new medications. Used in Medicinal Development: This chemical is employed as a precursor or building block in the synthesis of various therapeutic agents, potentially leading to the creation of antiviral, antibacterial, or antifungal medications. Used in Material Science: Given its unique chemical structure and potential reactivity, 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)may also find applications in material science, where its properties could be harnessed for specific material properties or functions. Used in Chemical Synthesis: 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)may serve as an intermediate or reactant in chemical synthesis processes, where its reactivity and structural features could be exploited to produce a range of other chemical products.

What is the CAS number for 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)-?

The CAS number of 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)- is 7118-63-0.

1H-Benzimidazole, 5-chloro-2-(phenylmethyl)-

Q: What is 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)- (7118-63-0) used for?

1H-Benzimidazole, 5-chloro-2-(phenylmethyl)is a chemical compound characterized by a benzene ring fused to an imidazole ring, featuring a chlorine atom and a phenylmethyl group at distinct positions on the benzimidazole structure. 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)is recognized for its potential in pharmaceutical research as a drug candidate due to its structural resemblance to biologically active molecules.

Base Information

Chemical Name:1H-Benzimidazole, 5-chloro-2-(phenylmethyl)-
CAS No.:7118-63-0

Factory supply 1H-Benzimidazole, 5-chloro-2-(phenylmethyl)- 7118-63-0 with sufficient stock and high standard

Molecular Formula:C14H11ClN2
Molecular Weight:242.708

7118-63-0 Relevant articles

Reactions of 2-carbonyl- And 2-hydroxy(or methoxy)alkylsubstituted benzimidazoles with arenes in the superacid CF3SO3H. NMR and DFT studies of dicationic electrophilic species

Ryabukhin, Dmitry S.,Turdakov, Alexey N.,Soldatova, Natalia S.,Kompanets, Mikhail O.,Ivanov, Alexander Yu.,Boyarskaya, Irina A.,Vasilyev, Aleksander V.

supporting information, p. 1962 - 1973 (2019/09/03)

Reactions of 2-carbonyl- and 2-hydroxy(o...

Decarboxylative Coupling of α-Keto Acids with ortho-Phenylenediamines Promoted by an Electrochemical Method in Aqueous Media

Wang, Hai-Bin,Huang, Jing-Mei

supporting information, p. 1975 - 1981 (2016/07/06)

An electrochemical method for the decarb...

Assembly of substituted 1H-benzimidazoles and 1,3-dihydrobenzimidazol-2- ones via CuI/L-proline catalyzed coupling of aqueous ammonia with 2-iodoacetanilides and 2-iodophenylcarbamates

Diao, Xiaoqiong,Wang, Yuji,Jiang, Yongwen,Ma, Dawei

experimental part, p. 7974 - 7977 (2010/02/28)

(Chemical Equation Presented) CuI/L-prol...

Preparation and pharmacologic activity of 2-(4'R')benzyl-5R-benzimidazole. Analgesic activity and effect on conditioned avoidance response

Paglietti,Pirisi,Loriga,Grella,Sparatore,Satta,Manca,Peana

, p. 203 - 214 (2007/10/02)

Several derivatives of 2-benzylbenzimida...

7118-63-0 Process route

: 6953-65-7
(5-chloro-1H-benzo [d]imidazol-2-yl)methanol

: 71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1
benzene

: 7118-63-0
2-benzyl-5-chloro-1H-benzo[d]imidazole

Conditions

Conditions	Yield
With trifluorormethanesulfonic acid; at 140 ℃; for 2.5h;	88%

: 5-chloro-2-(methoxymethyl)-1H-benzimidazole

: 71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1
benzene

: 7118-63-0
2-benzyl-5-chloro-1H-benzo[d]imidazole

Conditions

Conditions	Yield
With trifluorormethanesulfonic acid; at 140 ℃; for 2.5h;	52%

7118-63-0 Upstream products

7118-58-3
N-(p-chlorophenyl)phenylacetamidine
5442-34-2
ethyl 2-phenylacetimidate hydrochloride
95-83-0
4-Chloro-1,2-phenylenediamine
1016503-51-7
C₁₄H₁₃ClN₂O

7118-63-0 Downstream products

91709-07-8
N-<(2,4-dinitrophenyl)thio>-2-benzyl-5-chlorobenzimidazole

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