Cas 132589-67-4,2-(2,2-Dimethyl-propionyl)-6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-one

132589-67-4

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Basic information

Product Name: 2-(2,2-Dimethyl-propionyl)-6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-one
Synonyms: 2-(2,2-Dimethyl-propionyl)-6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-one
CAS NO:132589-67-4
Molecular Formula:
Molecular Weight: 291.347
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: 2-(2,2-Dimethyl-propionyl)-6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2,2-Dimethyl-propionyl)-6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-one(132589-67-4)
EPA Substance Registry System: 2-(2,2-Dimethyl-propionyl)-6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-one(132589-67-4)

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: 132589-67-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132589-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,8 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132589-67:
(8*1)+(7*3)+(6*2)+(5*5)+(4*8)+(3*9)+(2*6)+(1*7)=144
144 % 10 = 4
So 132589-67-4 is a valid CAS Registry Number.

132589-67-4Upstream product

132589-67-4Downstream Products

493-49-2 6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-one

132589-67-4Relevant academic research and scientific papers

Unusual Formation of Tetrahydro-1-isoquinolones from Tetrahydroisoquinoline-1-carboxylic Acids with Carbodiimides and Mechanistic Aspects

Kawase, Masami

, p. 1328 - 1329 (2007/10/02)

The reaction of tetrahydroisoquinoline-1-carboxylic acids with carbodiimides leads to the formation of tetrahydro-1-isoquinolones in high yields, involving a reaction between mesoionic 1,3-oxazol-5-one intermediates and molecular oxygen.

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