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5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI), also known as dihydropyridinone, is a heterocyclic chemical compound with the molecular formula C6H7NO. It features a cyclopentane ring fused to a pyridine ring and a ketone functional group. 5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI) is widely used in organic synthesis as a building block for the preparation of various pharmaceuticals and biologically active compounds. Its unique structure and reactivity have garnered interest in its potential anti-inflammatory and anti-cancer properties, making it a valuable intermediate in the development of new drugs and agrochemicals.

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  • 350847-80-2 Structure
  • Basic information

    1. Product Name: 5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI)
    2. Synonyms: 5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI);6,7-Dihydro-5H-[2]pyrindin-5-one;6,7-dihydro-5H-cyclopenta[c]pyridin-5-one;6,7-Dihydro-5H-cyclopental[c]pyridine-5-one;6,7-dihydrocyclopenta[c]pyridin-5-one;6,7-Dihydro-5H-cyclopental[c]pyridin-5-one;5H,6H,7H-cyclopenta[c]pyridin-5-one;5H-Cyclopenta[c]pyridin-5-one, 6,7-dihydro-
    3. CAS NO:350847-80-2
    4. Molecular Formula: C8H7NO
    5. Molecular Weight: 133.149
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 350847-80-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 267.379 °C at 760 mmHg
    3. Flash Point: 122.62 °C
    4. Appearance: /
    5. Density: 1.23 g/cm3
    6. Vapor Pressure: 0.008mmHg at 25°C
    7. Refractive Index: 1.592
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 3.56±0.20(Predicted)
    11. CAS DataBase Reference: 5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI)(CAS DataBase Reference)
    12. NIST Chemistry Reference: 5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI)(350847-80-2)
    13. EPA Substance Registry System: 5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI)(350847-80-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 350847-80-2(Hazardous Substances Data)

350847-80-2 Usage

Uses

Used in Pharmaceutical Industry:
5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals for its potential anti-inflammatory and anti-cancer properties. Its unique structure allows for the development of new drugs with improved efficacy and reduced side effects.
Used in Organic Synthesis:
In the field of organic synthesis, 5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI) serves as a versatile building block for the preparation of a wide range of biologically active compounds. Its reactivity and structural features enable the creation of diverse molecules with potential applications in various industries.
Used in Agrochemical Development:
5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI) is also utilized in the development of new agrochemicals, where its unique properties can contribute to the creation of more effective and environmentally friendly products for agricultural applications.
Used in Research and Development:
Due to its potential anti-inflammatory and anti-cancer properties, 5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-(9CI) is extensively used in research and development for the discovery of novel therapeutic agents and the advancement of drug design strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 350847-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,0,8,4 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 350847-80:
(8*3)+(7*5)+(6*0)+(5*8)+(4*4)+(3*7)+(2*8)+(1*0)=152
152 % 10 = 2
So 350847-80-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO/c10-8-2-1-6-5-9-4-3-7(6)8/h3-5H,1-2H2

350847-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-dihydrocyclopenta[c]pyridin-5-one

1.2 Other means of identification

Product number -
Other names 6,7-Dihydro-[2]pyrindin-5-one

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:350847-80-2 SDS

350847-80-2Downstream Products

350847-80-2Relevant articles and documents

Effect of copper(II) triflate on intramolecular Diels-Alder reaction of oxazole-olefins

Ohba, Masashi,Izuta, Rie

, p. 823 - 826 (2001)

Intramolecular Diels - Alder reaction of the oxazole-olefins (8a) and (11a) was effectively promoted by addition of a catalytic amount of copper(II) triflate to afford the cyclopenta[c]pyridines (9a) and (12a), respectively.

PLASMA KALLIKREIN INHIBITORS AND USES THEREOF

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Paragraph 0900; 0904, (2021/03/19)

The present invention provides compounds and compositions thereof which are useful as inhibitors of plasma kallikrein and which exhibit desirable characteristics for the same.

DUAL NAV1.2/5HT2A INHIBITORS FOR TREATING CNS DISORDERS

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Paragraph 0132; 0134; 0283, (2018/03/28)

Compounds of formula I: I are disclosed, as are pharmaceutical compositions containing such compounds. Methods of treating neurological or psychiatric disorders in a patient in need are also disclosed. Such disorders include depression, bipolar disorder, pain, schizophrenia, obsessive compulsive disorder, addiction, social disorder, attention deficit hyperactivity disorder, an anxiety disorder, autism, a cognitive impairment, or a neuropsychiatric symptom such as apathy, depression, anxiety, psychosis, aggression, agitation, impulse control disorders, and sleep disorders in neurological disorders such as Alzheimer's and Parkinson's diseases.

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