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6,7-dimethoxy-1-(3,4,5-trimethoxyphenyl)-3,4-dihydroisoquinoline is a complex organic compound belonging to the isoquinoline family. It is characterized by a dihydroisoquinoline core, which is a reduced form of isoquinoline, and features a phenyl ring substituted with three methoxy groups at positions 3, 4, and 5. The compound also has two methoxy groups at positions 6 and 7 of the dihydroisoquinoline ring. This molecule is known for its potential applications in medicinal chemistry, particularly in the development of drugs targeting the central nervous system. Its unique structure and functional groups make it an interesting subject for further research and development in the field of pharmaceuticals.

3161-21-5

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3161-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3161-21-5 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, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3161-21:
(6*3)+(5*1)+(4*6)+(3*1)+(2*2)+(1*1)=55
55 % 10 = 5
So 3161-21-5 is a valid CAS Registry Number.

3161-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-dimethoxy-1-(3,4,5-trimethoxyphenyl)-3,4-dihydroisoquinoline

1.2 Other means of identification

Product number -
Other names 1-<3',4',5'-Trimethoxyphenyl>-6,7-dimethoxy-3,4-dihydro-isochinolin

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:3161-21-5 SDS

3161-21-5Relevant academic research and scientific papers

Josiphos-Type Binaphane Ligands for Iridium-Catalyzed Enantioselective Hydrogenation of 1-Aryl-Substituted Dihydroisoquinolines

Nie, Huifang,Zhu, Yupu,Hu, Xiaomu,Wei, Zhao,Yao, Lin,Zhou, Gang,Wang, Pingan,Jiang, Ru,Zhang, Shengyong

supporting information, p. 8641 - 8645 (2019/10/17)

Convenient synthesis and useful application of a series of Josiphos-type binaphane ligands were described. The iridium complexes of these chiral diphosphines displayed excellent enantioselectivity and good reactivity in the asymmetric hydrogenation of challenging 1-aryl-substituted dihydroisoquinoline substrates (full conversions, up to >99% ee, 4000 TON). The use of 40% HBr (aqueous solution) as an additive dramatically improved the asymmetric induction of these catalysts. This transformation provided a highly efficient and enantioselective access to chiral 1-aryl-substituted tetrahydroisoquinolines, which were of great importance and common in natural products and biologically active molecules.

Cerium Chloride Catalyzed, 2-Iodoxybenzoic Acid Mediated Oxidative Dehydrogenation of Multiple Heterocycles at Room Temperature

Hati, Santanu,Sen, Subhabrata

supporting information, p. 1277 - 1280 (2017/03/17)

Catalytic cerium chloride was found to activate 2-iodoxybenzoic acid (IBX) for the oxidative dehydrogenation of tetrahydroisoquinolines, tetrahydro-β-carbolines, and thiazolidines to their dehydrogenated and aromatic forms at room temperature in moderate to excellent yields. The robustness of the protocol was demonstrated by scaling up the reactions to multigram quantities.

Total synthesis of racemic 1-aryl-tetrahydroisoquinoline alkaloids

ábrányi-Balogh, Péter,F?ldesi, Tamás,Milen, Mátyás

, p. 1907 - 1912 (2015/10/29)

A new synthetic route was developed for the preparation of natural products cryptostyline I, II, III and 1-phenyl-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline. The Liebeskind-Srogl palladium-catalyzed carbon-carbon cross-coupling protocol was use

A highly efficient and enantioselective access to tetrahydroisoquinoline alkaloids: Asymmetric hydrogenation with an iridium catalyst

Chang, Mingxin,Li, Wei,Zhang, Xumu

supporting information; experimental part, p. 10679 - 10681 (2011/12/05)

Efficient and enantioselective: Using the iodine-bridged dimeric iridium complex [{Ir(H)[(S,S)-(f)-binaphane]}2(μ-I)3] +I- (1) a wide range of tetrahydroisoquinoline alkaloids, including the substructure of the pharmaceutical drug solifenacin, were obtained with excellent enantioselectivities and high turnover numbers (see scheme). Copyright

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