CAS 855778-84-6

Chemistry, 1 End Use API, 4 Related Intermediates

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Also known as: 855778-84-6, Schembl2209444, Bapaubkdzoewjl-uhfffaoysa-n, E72264, 3-(piperidin-4-yl)quinolin-2(1h)-one-hydrochloride, 3-(4-piperidinyl)-2(1h)-quinolinone hydrochloride

Molecular Formula

C₁₄H₁₇ClN₂O

Molecular Weight

264.75 g/mol

InChI Key

BAPAUBKDZOEWJL-UHFFFAOYSA-N

1 2D Structure

CAS 855778-84-6

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

3-piperidin-4-yl-1H-quinolin-2-one;hydrochloride

2.1.2 InChI

InChI=1S/C14H16N2O.ClH/c17-14-12(10-5-7-15-8-6-10)9-11-3-1-2-4-13(11)16-14;/h1-4,9-10,15H,5-8H2,(H,16,17);1H

2.1.3 InChI Key

BAPAUBKDZOEWJL-UHFFFAOYSA-N

2.1.4 Canonical SMILES

C1CNCCC1C2=CC3=CC=CC=C3NC2=O.Cl

2.2 Synonyms

2.2.1 Depositor-Supplied Synonyms

1. 855778-84-6

2. Schembl2209444

3. Bapaubkdzoewjl-uhfffaoysa-n

4. E72264

5. 3-(piperidin-4-yl)quinolin-2(1h)-one-hydrochloride

6. 3-(4-piperidinyl)-2(1h)-quinolinone Hydrochloride

2.3 Create Date

2012-11-30

3 Chemical and Physical Properties

Molecular Formula	C₁₄H₁₇ClN₂O
Molecular Weight	264.75 g/mol
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	1
Exact Mass	g/mol
Monoisotopic Mass	g/mol
Topological Polar Surface Area	41.1
Heavy Atom Count	18
Formal Charge	0
Complexity	331
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	2

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Vamsi Labs

Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.

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N-Methyl-4- Piperidone

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1445-73-4

End Use API

Vamsi Labs, established in 1991, is a leading Indian API manufacturer. Specializing in anti-asthmatic, an...

Vamsi Labs, established in 1991, is a leading Indian API manufacturer. Specializing in anti-asthmatic, anti-migraine & anti-psychotic APIs, it caters to domestic & international markets(50% sales). Anti-asthma products account for 60% of sales. Vamsi adheres to high corporate governance, transparency, professionalism, & environmental protection standards. It's USFDA approved & ISO 9001:2015, ISO 14001:2015, & ISO 45001:2018 certified. With a DSIR-certified R&D Lab, Vamsi continues to innovate & meet the pharma industry's evolving needs. Vamsi is poised to grow its globally while maintaining its commitment to excellence and sustainability.

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Tagoor Laboratories

Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.

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India

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N-Methyl-4-piperidone

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1445-73-4

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Tagoor Laboratories, established in 2018, is a part of the Tagoor Group. It specializes in providing APIs...

Tagoor Laboratories, established in 2018, is a part of the Tagoor Group. It specializes in providing APIs, advanced intermediates and key starting materials for critical and high-growth therapeutic areas, with an emphasis on affordability, quality and timely delivery. It also provides end-to-end CDMO services. Headquartered in Hyderabad, Tagoor Labs is a fast-growing Indian pharma company that serves both branded and generic companies worldwide. The company’s organizational function includes R&D, supply chain, manufacturing, quality testing, quality assurance, regulatory affairs, marketing & sales, and packaging & warehousing departments.

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Porton Pharma Solutions

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China

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Methyl (2R)-2-amino-3-(7- methyl-1H-indazol-5- yl)propa...

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1414976-14-9

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Zavegepant

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Porton Pharma Solutions Ltd. was founded in 2005, & the company's stock was successfully listed in Shenzh...

Porton Pharma Solutions Ltd. was founded in 2005, & the company's stock was successfully listed in Shenzhen Stock Exchange in 2014. Our R&D, manufacturing & operation facilities are located in China, Slovenia, the US, Belgium, Switzerland, Denmark, with more than 6000 employees worldwide. Porton leads the way with its excellent CDMO services, but also supplies APIs & intermediates for the treatment of critical diseases such as HIV/AIDS, diabetes, cancer, & influenza. Our Process Technology Centers & WHO/USFDA/EMA/PDMA/NMPA-inspected Facilities feature state-of-the-art equipment, highly flexible cGMP-compliant production assets.

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