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3-Piperidineacetonitrile, also known as 3-Cyanomethylpiperidine, is an organic compound that serves as a crucial intermediate in the synthesis of various pharmaceuticals. It is characterized by its piperidine ring and cyanomethyl group, which contribute to its reactivity and potential applications in the medical field.

5562-22-1

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5562-22-1 Usage

Uses

Used in Pharmaceutical Industry:
3-Piperidineacetonitrile is used as a key intermediate for the synthesis of 2,4,6-trisubstituted pyrimidines. These compounds are known as phosphatidylinositol 3-kinase (PI3 kinase) inhibitors, which play a significant role in the treatment of cancer. By targeting the PI3 kinase pathway, these inhibitors can help regulate cell growth and survival, making them valuable tools in the fight against cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 5562-22-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5562-22:
(6*5)+(5*5)+(4*6)+(3*2)+(2*2)+(1*2)=91
91 % 10 = 1
So 5562-22-1 is a valid CAS Registry Number.

5562-22-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-piperidin-3-ylacetonitrile

1.2 Other means of identification

Product number -
Other names 3-Cyanomethylpiperidine

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:5562-22-1 SDS

5562-22-1Relevant academic research and scientific papers

Structure-activity relationship study of tryptophan-based butyrylcholinesterase inhibitors

Brazzolotto, Xavier,Gobec, Stanislav,Gro?elj, Uro?,Knez, Damijan,Malikowska-Racia, Natalia,Meden, An?e,Nachon, Florian,Sa?at, Kinga,Svete, Jurij

, (2020/09/15)

A series of tryptophan-based selective nanomolar butyrylcholinesterase (BChE) inhibitors was designed and synthesized. Compounds were optimized in terms of potency, selectivity, and synthetic accessibility. The crystal structure of the inhibitor 18 in complex with BChE revealed the molecular basis for its low nanomolar inhibition (IC50 = 2.8 nM). The favourable in vitro results enabled a first-in-animal in vivo efficacy and safety trial, which demonstrated a positive impact on fear-motivated and spatial long-term memory retrieval without any concomitant adverse motor effects. Altogether, this research culminated in a handful of new lead compounds with promising potential for symptomatic treatment of patients with Alzheimer's disease.

Amino substituted dibenzothiophene derivatives for the treatment of disorders mediated by np y5 receptor

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Page 53, (2010/02/05)

Compounds of formula (I): wherein: X is a group of formula (A) or (B): and R1, R2, R3, R4, n, x, y and z are as defined within are described. Processes for their preparation and their use in the treatment of disorders mediated by the neuropeptide Y5 receptor in a warm-blooded animal, such as a human being are also described.

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