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6,7-dimethoxy-1-pyridin-3-yl-1,2,3,4-tetrahydroisoquinoline is a complex organic compound with a molecular formula of C18H20N2O2. It is a derivative of isoquinoline, a heterocyclic aromatic organic compound with a bicyclic structure consisting of a benzene ring fused to a pyridine ring. The compound features two methoxy groups at the 6 and 7 positions, and a pyridin-3-yl group at the 1 position. The tetrahydroisoquinoline part of the molecule indicates that the isoquinoline ring has undergone hydrogenation, resulting in a saturated six-membered ring. 6,7-dimethoxy-1-pyridin-3-yl-1,2,3,4-tetrahydroisoquinoline has potential applications in the field of medicinal chemistry, particularly in the development of drugs targeting the central nervous system, due to its unique structure and potential interactions with various biological targets.

3161-08-8

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3161-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3161-08-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,6 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3161-08:
(6*3)+(5*1)+(4*6)+(3*1)+(2*0)+(1*8)=58
58 % 10 = 8
So 3161-08-8 is a valid CAS Registry Number.

3161-08-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-dimethoxy-1-(pyridin-3-yl)-1,2,3,4-tetrahydroisoquinoline

1.2 Other means of identification

Product number -
Other names 6,7-dimethoxy-1-pyridin-3-yl-1,2,3,4-tetrahydroisoquinoline 1.5H2C2O4

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:3161-08-8 SDS

3161-08-8Downstream Products

3161-08-8Relevant academic research and scientific papers

Complete assignments 1H and13C NMR spectral data of four anabaseine derivatives

Sobarzo-Sanchez, Eduardo,De La Fuente, Julio,Quezada, Elias,Castedo, Luis

, p. 1131 - 1134 (2006)

The anabaseine derivatives 6-methoxy-7-hydroxy-1-(pyridin-3-yl)-3,4- dihydroisoquinoline, 6,7-dimethoxy-1-(pyridin-3-yl)-1,2,3,4- tetrahydroisoqumoline and 6,7-dimethoxy-1-(piperidin-3-yl)-1,2,3,4- tetrahydroisoquinoline were prepared either by demethylation with HBr or by reduction with different reagents, NaBH4 and H2/PtO 2 from 6,7-dimethoxy-1-(pyridin-3-yl)-3,4-dihydroisoquinoline, as starting material. The structures have been fully assigned by the combination of one- and two-dimensional experiments. Copyright

Synthesis of anabaseine and anabasine derivatives: Structural modifications of possible nicotinic agonists

Sobarzo-Sanchez, Eduardo,Castedo, Luis,De La Fuente, Julio R.

, p. 1331 - 1338 (2008/02/01)

Coupling nicotinoyl chloride with 3,4-dimetoxyphenethylamine under Bischler-Napieralski cyclization afforded the isoquinoline (4) in good yield. This latter was used as starting material to obtain with only hydrobromic acid a product with demethylation at

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