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α-(1-Methyl-1H-benzimidazole-2-yl)-4-bromobenzyl alcohol is a unique chemical compound characterized by a benzimidazole group with a methyl substituent on the nitrogen atom, connected to a 4-bromobenzyl alcohol molecule. This distinctive structure endows the compound with potential applications in drug discovery and medicinal chemistry, given the known pharmacological properties of the benzimidazole core, such as antiparasitic, antifungal, and anticancer effects. The bromine atom in the benzyl alcohol moiety may further modify the compound's interactions with target molecules, possibly enhancing or altering its biological activity.

7104-68-9

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7104-68-9 Usage

Uses

Used in Pharmaceutical Industry:
α-(1-Methyl-1H-benzimidazole-2-yl)-4-bromobenzyl alcohol is used as a potential drug candidate for various therapeutic applications due to its benzimidazole core, which is known to exhibit antiparasitic, antifungal, and anticancer properties. α-(1-Methyl-1H-benzimidazole-2-yl)-4-bromobenzyl alcohol's unique structure may offer new avenues for drug development, particularly in the treatment of parasitic infections, fungal diseases, and cancer.
Used in Medicinal Chemistry Research:
α-(1-Methyl-1H-benzimidazole-2-yl)-4-bromobenzyl alcohol serves as a valuable compound for medicinal chemistry research, where its unique structure and potential biological activities can be further explored and optimized. α-(1-Methyl-1H-benzimidazole-2-yl)-4-bromobenzyl alcohol's interactions with target molecules can be studied to understand its mechanism of action and to develop more effective and selective drugs.
Used in Drug Design and Optimization:
α-(1-Methyl-1H-benzimidazole-2-yl)-4-bromobenzyl alcohol is utilized in drug design and optimization processes, where its unique structure can be modified or combined with other chemical moieties to enhance its biological activity, selectivity, and pharmacokinetic properties. This may lead to the development of novel drugs with improved therapeutic potential.
Further research and testing are required to fully understand the potential uses and effects of α-(1-Methyl-1H-benzimidazole-2-yl)-4-bromobenzyl alcohol in various applications, as its exact role and mechanism of action in different biological systems are yet to be elucidated.

Check Digit Verification of cas no

The CAS Registry Mumber 7104-68-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,0 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7104-68:
(6*7)+(5*1)+(4*0)+(3*4)+(2*6)+(1*8)=79
79 % 10 = 9
So 7104-68-9 is a valid CAS Registry Number.

7104-68-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-bromo-phenyl)-(1-methyl-1H-benzoimidazol-2-yl)-methanol

1.2 Other means of identification

Product number -
Other names 1-Methyl-2-(4-brom-α-hydroxybenzyl)-benzimidazol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7104-68-9 SDS

7104-68-9Upstream product

7104-68-9Downstream Products

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