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Cyclopropyl(3-pyridyl) ketone is a chemical compound with the molecular formula C10H11NO. It is a combination of cyclopropane (a three-carbon ring) and 3-pyridyl group (a nitrogen-containing ring), with a ketone functional group (carbon double-bonded to oxygen). As such, it has properties common to aromatic compounds, ketones, and cyclopropane derivatives.

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  • 24966-13-0 Structure
  • Basic information

    1. Product Name: Cyclopropyl(3-pyridyl) ketone
    2. Synonyms: Cyclopropyl(3-pyridyl) ketone;cyclopropyl(3-pyridinyl)methanone(SALTDATA: FREE);cyclopropyl(3-pyridinyl)methanone;Cyclopropyl(3-pyridyl)Methanone;cyclopropyl(pyridin-3-yl)methanone;METHANONE, CYCLOPROPYL-3-PYRIDINYL-
    3. CAS NO:24966-13-0
    4. Molecular Formula: C9H9NO
    5. Molecular Weight: 147.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24966-13-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 272.7°C at 760 mmHg
    3. Flash Point: 126°C
    4. Appearance: /
    5. Density: 1.191g/cm3
    6. Vapor Pressure: 0.00598mmHg at 25°C
    7. Refractive Index: 1.588
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 3.27±0.10(Predicted)
    11. CAS DataBase Reference: Cyclopropyl(3-pyridyl) ketone(CAS DataBase Reference)
    12. NIST Chemistry Reference: Cyclopropyl(3-pyridyl) ketone(24966-13-0)
    13. EPA Substance Registry System: Cyclopropyl(3-pyridyl) ketone(24966-13-0)
  • Safety Data

    1. Hazard Codes: T
    2. Statements: 25
    3. Safety Statements: 45
    4. RIDADR: UN 2811 6.1 / PGIII
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 24966-13-0(Hazardous Substances Data)

24966-13-0 Usage

Uses

Used in Pharmaceutical Industry:
Cyclopropyl(3-pyridyl) ketone is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of new molecules with potential therapeutic applications.
Used in Experimental Organic Chemistry:
Cyclopropyl(3-pyridyl) ketone is used as a research compound in experimental organic chemistry. Its properties and reactivity can be studied to gain insights into the behavior of similar compounds and to develop new synthetic methods or reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 24966-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,6 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24966-13:
(7*2)+(6*4)+(5*9)+(4*6)+(3*6)+(2*1)+(1*3)=130
130 % 10 = 0
So 24966-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO/c11-9(7-3-4-7)8-2-1-5-10-6-8/h1-2,5-7H,3-4H2

24966-13-0 Well-known Company Product Price

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  • Aldrich

  • (CBR00500)  Cyclopropyl(3-pyridinyl)methanone  AldrichCPR

  • 24966-13-0

  • CBR00500-1G

  • 2,767.05CNY

  • Detail

24966-13-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopropyl(pyridin-3-yl)methanone

1.2 Other means of identification

Product number -
Other names Cyclopropyl-3-pyridyl-keton

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:24966-13-0 SDS

24966-13-0Downstream Products

24966-13-0Relevant articles and documents

2-Pyridyl and 3-pyridylzinc bromides: direct preparation and coupling reaction

Kim, Seung-Hoi,Rieke, Reuben D.

scheme or table, p. 3135 - 3146 (2010/06/13)

A facile synthetic approach to the direct preparation of 2-pyridyl and 3-pyridylzinc bromides has been demonstrated using Rieke zinc with 2-bromopyridine and 3-bromopyridine, respectively. A variety of different electrophiles have been coupled with the resulting organozinc reagents to give the corresponding cross-coupling products in moderate to good yields.

A facile synthetic approach to the preparation of 3-pyridyl derivatives: Preparations and coupling reactions of 3-pyridylzinc and its analogues

Kim, Seung-Hoi,Slocum, Tim B.,Rieke, Reuben D.

experimental part, p. 3823 - 3827 (2010/03/04)

A facile synthetic approach to the direct preparation of 3pyridylzinc bromide has been demonstrated using Rieke zinc with 3-bromopyridine in the presence of a catalytic amount of lithium chloride. A variety of different electrophiles have been coupled to give the corresponding cross-coupling products in moderate to good yields. Also, this methodology has been expanded to the preparation of the corresponding organozinc reagents of 3-bromopyridine analogues. Georg Thieme Verlag Stuttgart.

Branched alkylamino derivatives of thiazole, processes for preparing them and pharmaceutical compositions containing them

-

, (2008/06/13)

The invention relates to the derivatives of formula I: STR1 in which R1 represents a phenyl or naphthyl radical (optionally substituted), R2 represents a hydrogen or halogen atom or an alkyl, hydroxymethyl or formyl radical, R3

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