Cas 16624-97-8,(S)-9-[2-((R)-6,7-Dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinolin-1-ylmethyl)-4,5-dimethoxy-phenoxy]-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline

16624-97-8

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Basic information

Product Name: (S)-9-[2-((R)-6,7-Dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinolin-1-ylmethyl)-4,5-dimethoxy-phenoxy]-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline
Synonyms:
CAS NO:16624-97-8
Molecular Formula:
Molecular Weight: 696.841
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S)-9-[2-((R)-6,7-Dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinolin-1-ylmethyl)-4,5-dimethoxy-phenoxy]-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline(CAS DataBase Reference)
NIST Chemistry Reference: (S)-9-[2-((R)-6,7-Dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinolin-1-ylmethyl)-4,5-dimethoxy-phenoxy]-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline(16624-97-8)
EPA Substance Registry System: (S)-9-[2-((R)-6,7-Dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinolin-1-ylmethyl)-4,5-dimethoxy-phenoxy]-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline(16624-97-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 16624-97-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 16624-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,2 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16624-97:
(7*1)+(6*6)+(5*6)+(4*2)+(3*4)+(2*9)+(1*7)=118
118 % 10 = 8
So 16624-97-8 is a valid CAS Registry Number.

16624-97-8Upstream product

74-88-4 methyl iodide

16624-97-8Downstream Products

16624-97-8Relevant academic research and scientific papers

Catalytic Aerobic Cross-Dehydrogenative Coupling of Phenols and Catechols

Xu, Wenbo,Huang, Zheng,Ji, Xiang,Lumb, Jean-Philip

, p. 3800 - 3810 (2019)

We describe a selective, catalytic aerobic cross-dehydrogenative coupling (CDC) reaction of phenols and catechols that creates aryl ethers. To avoid challenges of selectivity, we employ copper (Cu) coordination to confine substrate redox to the inner coor

Compounds and compositions for treating infection

-

, (2009/04/24)

Compounds from 14 Kenyan plants, including from the root of Dovyalis abyssinica and Clutia robusta have been characterized and isolated, and their uses are disclosed.

Isoquinoline compounds

-

, (2008/06/13)

There is disclosed a novel total synthesis of Thalicarpine which includes inter alia a total synthesis of hernandaline. The novel process is characterized in utilizing simple and readily available starting materials to form a diaryl ether system which is

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