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4-BOC-AMINO-1-[1-(4-FLUORO-BENZYL)-1H-BENZOIMIDAZOL-2-YL]-PIPERIDINE is a complex organic chemical compound that is part of the piperidine class. It features a piperidine ring with an amino group and a benzimidazole moiety attached. The benzimidazole ring is substituted with a fluorobenzyl group, and the amino group is protected by a BOC (tert-butoxycarbonyl) group. 4-BOC-AMINO-1-[1-(4-FLUORO-BENZYL)-1H-BENZOIMIDAZOL-2-YL]-PIPERIDINE holds promise in the fields of medicinal chemistry and drug development due to its potential role in the synthesis of pharmaceuticals and bioactive molecules. Its unique structural features may also endow it with biological activity, allowing it to bind to specific receptors or enzymes.

885270-85-9

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885270-85-9 Usage

Uses

Used in Medicinal Chemistry:
4-BOC-AMINO-1-[1-(4-FLUORO-BENZYL)-1H-BENZOIMIDAZOL-2-YL]-PIPERIDINE is used as a key intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs with specific therapeutic targets.
Used in Drug Development:
In the pharmaceutical industry, 4-BOC-AMINO-1-[1-(4-FLUORO-BENZYL)-1H-BENZOIMIDAZOL-2-YL]-PIPERIDINE serves as a building block in the creation of bioactive molecules, which can be further modified to enhance their efficacy and selectivity in treating various diseases.
Used in Biological Research:
4-BOC-AMINO-1-[1-(4-FLUORO-BENZYL)-1H-BENZOIMIDAZOL-2-YL]-PIPERIDINE is utilized as a research tool in biological studies to investigate its binding affinity to specific receptors or enzymes, which can provide insights into its potential therapeutic applications.
Used in Chemical Synthesis:
4-BOC-AMINO-1-[1-(4-FLUORO-BENZYL)-1H-BENZOIMIDAZOL-2-YL]-PIPERIDINE is employed as a synthetic precursor in organic chemistry, allowing for the creation of a variety of complex molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 885270-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 885270-85:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*0)+(2*8)+(1*5)=209
209 % 10 = 9
So 885270-85-9 is a valid CAS Registry Number.

885270-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 2-amino-1-[1-[(4-fluorophenyl)methyl]benzimidazol-2-yl]piperidine-4-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:885270-85-9 SDS

885270-85-9Downstream Products

885270-85-9Relevant academic research and scientific papers

Brain-penetrating 2-aminobenzimidazole H1-antihistamines for the treatment of insomnia

Coon, Timothy,Moree, Wilna J.,Li, Binfeng,Yu, Jinghua,Zamani-Kord, Said,Malany, Siobhan,Santos, Mark A.,Hernandez, Lisa M.,Petroski, Robert E.,Sun, Aixia,Wen, Jenny,Sullivan, Sue,Haelewyn, Jason,Hedrick, Michael,Hoare, Samuel J.,Bradbury, Margaret J.,Crowe, Paul D.,Beaton, Graham

scheme or table, p. 4380 - 4384 (2010/04/05)

The benzimidazole core of the selective non-brain-penetrating H1-antihistamine mizolastine was used to identify a series of brain-penetrating H1-antihistamines for the potential treatment of insomnia. Using cassette PK studies, brain

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