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5-Fluorobenzimidazole-2-carboxaldehyde is a chemical compound characterized by a benzimidazole ring with a fluorine atom and an aldehyde group. It is recognized for its reactivity and serves as a crucial intermediate in the synthesis of pharmaceuticals and agrochemicals. The unique structure and reactivity of 5-Fluorobenzimidazole-2-carboxaldehyde make it a significant building block in medicinal and agricultural chemistry, with potential applications in drug discovery, development, and crop protection.

885280-34-2

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885280-34-2 Usage

Uses

Used in Pharmaceutical Industry:
5-Fluorobenzimidazole-2-carboxaldehyde is used as a key intermediate for the synthesis of various pharmaceuticals. Its reactivity and unique structure contribute to the development of new drugs with improved therapeutic properties and efficacy.
Used in Agrochemical Industry:
5-Fluorobenzimidazole-2-carboxaldehyde is used as a building block in the synthesis of agrochemicals. It plays a vital role in the development of new crop protection agents, enhancing agricultural productivity and ensuring food security.
Used in Medicinal Chemistry:
5-Fluorobenzimidazole-2-carboxaldehyde is used as a reactive intermediate in the construction of complex organic molecules through multi-step synthesis processes. Its unique structure and reactivity make it an important component in the discovery and development of novel therapeutic agents.
Used in Drug Discovery:
5-Fluorobenzimidazole-2-carboxaldehyde is used as a starting material in drug discovery, enabling the design and synthesis of new chemical entities with potential therapeutic applications. Its unique properties facilitate the exploration of new chemical space and the identification of promising drug candidates.
Used in Crop Protection:
5-Fluorobenzimidazole-2-carboxaldehyde is used in the development of innovative agrochemicals for crop protection. Its incorporation into the synthesis of new pesticides and herbicides can lead to improved control of pests and diseases, ultimately contributing to increased crop yields and better agricultural sustainability.

Check Digit Verification of cas no

The CAS Registry Mumber 885280-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,8 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 885280-34:
(8*8)+(7*8)+(6*5)+(5*2)+(4*8)+(3*0)+(2*3)+(1*4)=202
202 % 10 = 2
So 885280-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H5FN2O/c9-5-1-2-6-7(3-5)11-8(4-12)10-6/h1-4H,(H,10,11)

885280-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluoro-1H-benzimidazole-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 6-FLUORO-1H-BENZOIMIDAZOLE-2-CARBALDEHYDE

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:885280-34-2 SDS

885280-34-2Upstream product

885280-34-2Downstream Products

885280-34-2Relevant articles and documents

6-beta(substituted)-(S)-hydroxymethylpenicillanic acids and derivatives thereof

-

, (2008/06/13)

Antibacterial penicillins of the formula STR1 or a pharmaceutically acceptable salt thereof wherein R1 is a heterocyclic group and R is hydrogen, the residue of certian carboxy protecting groups or the residue of an ester group readily hydrolyzable in vivo having activity against resistant organisms.

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