Cas 86970-91-4,(1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one

86970-91-4

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Basic information

Product Name: (1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one
Synonyms: (1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one
CAS NO:86970-91-4
Molecular Formula:
Molecular Weight: 325.364
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: (1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one(86970-91-4)
EPA Substance Registry System: (1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one(86970-91-4)

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: 86970-91-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86970-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,7 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86970-91:
(7*8)+(6*6)+(5*9)+(4*7)+(3*0)+(2*9)+(1*1)=184
184 % 10 = 4
So 86970-91-4 is a valid CAS Registry Number.

86970-91-4Upstream product

86970-91-4Downstream Products

86970-95-8 threo-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-α-phenyl-1-isoquinolinemethanol

86970-91-4Relevant academic research and scientific papers

An efficient silver tetrafluoroborate-catalyzed cycloisomerization of ynamides

Ieawsuwan, Winai,Ruchirawat, Somsak

, p. 100 - 110 (2019)

A silver catalyzed-cycloisomerization of N-Boc protected ynamides has been developed under mild reaction conditions to provide a wide range of oxazol-2(3H)-ones in good to excellent yields. Moreover, the acid-promoted Pictet-Spengler cyclization of oxazol

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