Cas 723252-00-4,(8,9-dimethoxy-1-phenyl-1,5,6,10b-tetrahydro[1,2,4]triazolo[3,4-a]isoquinolin-3-yl)(2-thienyl)methanone

723252-00-4

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Basic information

Product Name: (8,9-dimethoxy-1-phenyl-1,5,6,10b-tetrahydro[1,2,4]triazolo[3,4-a]isoquinolin-3-yl)(2-thienyl)methanone
Synonyms: (8,9-dimethoxy-1-phenyl-1,5,6,10b-tetrahydro[1,2,4]triazolo[3,4-a]isoquinolin-3-yl)(2-thienyl)methanone
CAS NO:723252-00-4
Molecular Formula: C23H21N3O3S
Molecular Weight: 419.49614
EINECS: N/A
Product Categories: N/A
Mol File: 723252-00-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (8,9-dimethoxy-1-phenyl-1,5,6,10b-tetrahydro[1,2,4]triazolo[3,4-a]isoquinolin-3-yl)(2-thienyl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: (8,9-dimethoxy-1-phenyl-1,5,6,10b-tetrahydro[1,2,4]triazolo[3,4-a]isoquinolin-3-yl)(2-thienyl)methanone(723252-00-4)
EPA Substance Registry System: (8,9-dimethoxy-1-phenyl-1,5,6,10b-tetrahydro[1,2,4]triazolo[3,4-a]isoquinolin-3-yl)(2-thienyl)methanone(723252-00-4)

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: 723252-00-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 723252-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,3,2,5 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 723252-00:
(8*7)+(7*2)+(6*3)+(5*2)+(4*5)+(3*2)+(2*0)+(1*0)=124
124 % 10 = 4
So 723252-00-4 is a valid CAS Registry Number.

723252-00-4Upstream product

3382-18-1 6,7-dimethoxy-3,4-dihydro-isoquinoline

723252-00-4Downstream Products

723252-00-4Relevant academic research and scientific papers

Synthesis of [1,2,4]triazolo[3,4-a]isoquinolines and pyrrolo[2,1-a]isoquinolines using α-keto hydrazonoyl halides

Elwan, Nehal M.,Abdelhadi, Hyam A.,Abdallah, Taysser A.,Hassaneen, Hamdi M.

, p. 3451 - 3456 (1996)

Treatment of α-keto hydrazonoyl halides 1 with 3,4-dihydro-6,7-dimethoxyisoquinoline 3 and its 1-methyl derivative 4 in the presence of triethylamine in tetrahydrofuran at reflux afforded the corresponding cycloadducts 6 and 9, respectively. The same halides 1 react with 1-cyanomethyl-3,4-dihydro-6,7-dimethoxyisoquinoline 5 and afforded pyrrolo[2,1-a]isoquinoline derivatives 12 in high yield.

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