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Octahydro-2H-quinolizine-2-methanol is a cyclic amine alcohol with the chemical formula C10H19NO. It is a colorless to pale yellow liquid and is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Octahydro-2H-quinolizine-2-methanol is characterized by its octahydroquinolizine ring structure, which consists of a seven-membered ring with one nitrogen atom and two carbon atoms, and a hydroxyl group attached to the second carbon. Octahydro-2H-quinolizine-2-methanol is known for its versatile reactivity and is used in the preparation of various derivatives, making it a valuable building block in organic synthesis.

4968-90-5

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4968-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4968-90-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4968-90:
(6*4)+(5*9)+(4*6)+(3*8)+(2*9)+(1*0)=135
135 % 10 = 5
So 4968-90-5 is a valid CAS Registry Number.

4968-90-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxymethyl-chinolizidin

1.2 Other means of identification

Product number -
Other names (Octahydro-quinolizin-2-yl)-methanol

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:4968-90-5 SDS

4968-90-5Relevant academic research and scientific papers

Azabicyclic indole esters as potent 5-HT4 receptor antagonists

Wyman, Paul A.,Gaster, Laramie M.,King, Frank D.,Sutton, Jonathon M.,Ellis, Elizabeth S.,Wardle, Kay A.,Young, Timothy J.

, p. 255 - 261 (2007/10/03)

The synthesis of a series of azabicyclic indole esters is described and their potency reported as 5-HT4 receptor antagonists. Optimization of the most potent compound (19) by preparing the corresponding oxazino[3,2-a]indole ester afforded 34, which had a pIC50 of 9.5 in the guinea pig distal colon longitudinal muscle myenteric plexus preparation.

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