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OCTAHYDROQUINOLINE-4(1H)-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58869-89-9

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58869-89-9 Usage

Uses

Octahydro-4(1H)-quinolinone is used as pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 58869-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,6 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58869-89:
(7*5)+(6*8)+(5*8)+(4*6)+(3*9)+(2*8)+(1*9)=199
199 % 10 = 9
So 58869-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO/c11-9-5-6-10-8-4-2-1-3-7(8)9/h7-8,10H,1-6H2

58869-89-9 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H50180)  Octahydro-4(1H)-quinolinone, 97%   

  • 58869-89-9

  • 1g

  • 505.0CNY

  • Detail

  • Alfa Aesar

  • (H50180)  Octahydro-4(1H)-quinolinone, 97%   

  • 58869-89-9

  • 5g

  • 2269.0CNY

  • Detail

58869-89-9SDS

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 2,3,4a,5,6,7,8,8a-octahydro-1H-quinolin-4-one

1.2 Other means of identification

Product number -
Other names (+-)-trans-Octahydro-chinolin-4-on

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:58869-89-9 SDS

58869-89-9Relevant academic research and scientific papers

Decahydroquinoline amides as highly selective CB2 agonists: Role of selectivity on in vivo efficacy in a rodent model of analgesia

Manley, Peter J.,Zartman, Amy,Paone, Daniel V.,Burgey, Christopher S.,Henze, Darrell A.,Penna, Kimberly Della,Desai, Reshma,Leitl, Michael D.,Lemaire, Wei,White, Rebecca B.,Yeh, Suzie,Urban, Mark O.,Kane, Stefanie A.,Hartman, George D.,Bilodeau, Mark T.,Trotter, B. Wesley

scheme or table, p. 2359 - 2364 (2011/05/15)

A novel series of decahydroquinoline CB2 agonists is described. Optimization of the amide substituent led to improvements in CB2/CB1 selectivity as well as physical properties. Two key compounds were examined in the rat CFA model of acute inflammatory pain. A moderately selective CB2 agonist was active in this model. A CB2 agonist lacking functional CB1 activity was inactive in this model despite high in vivo exposure both peripherally and centrally.

DECAHYDROQUINOLINE ANALOGS AS CB2 RECEPTOR MODULATORS

-

Page/Page column 39, (2008/12/07)

The present invention relates to compounds represented by Formula (I): and pharmaceutically acceptable salts thereof. The present invention also provides pharmaceutical compositions comprising the instant compounds. This invention further provides methods to treat and prevent pain, respiratory and non-respiratory diseases.

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