Cas 78184-62-0,(14-hydroxy-14-phenyl-13b,14-dihydro-13aH-[1,3]benzothiazolo[2',3':3,4]pyrazino[2,1-c][1,4]benzothiazin-7-yl)(phenyl)methanone

78184-62-0

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Basic information

Product Name: (14-hydroxy-14-phenyl-13b,14-dihydro-13aH-[1,3]benzothiazolo[2',3':3,4]pyrazino[2,1-c][1,4]benzothiazin-7-yl)(phenyl)methanone
Synonyms: (14-hydroxy-14-phenyl-13b,14-dihydro-13aH-[1,3]benzothiazolo[2',3':3,4]pyrazino[2,1-c][1,4]benzothiazin-7-yl)(phenyl)methanone
CAS NO:78184-62-0
Molecular Formula: C₃₀H₂₂N₂O₂S₂
Molecular Weight: 506.63788
EINECS: N/A
Product Categories: N/A

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: (14-hydroxy-14-phenyl-13b,14-dihydro-13aH-[1,3]benzothiazolo[2',3':3,4]pyrazino[2,1-c][1,4]benzothiazin-7-yl)(phenyl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: (14-hydroxy-14-phenyl-13b,14-dihydro-13aH-[1,3]benzothiazolo[2',3':3,4]pyrazino[2,1-c][1,4]benzothiazin-7-yl)(phenyl)methanone(78184-62-0)
EPA Substance Registry System: (14-hydroxy-14-phenyl-13b,14-dihydro-13aH-[1,3]benzothiazolo[2',3':3,4]pyrazino[2,1-c][1,4]benzothiazin-7-yl)(phenyl)methanone(78184-62-0)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 78184-62-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78184-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,8 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78184-62:
(7*7)+(6*8)+(5*1)+(4*8)+(3*4)+(2*6)+(1*2)=160
160 % 10 = 0
So 78184-62-0 is a valid CAS Registry Number.

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78184-62-0Relevant academic research and scientific papers

CYCLOADDITION OF BENZOTHIAZOLIUM N-PHENACYLIDE WITH OLEFINIC DIPOLAROPHILES

Tsuge, Otohiko,Shimoharada, Hiroshi,Noguchi, Michihiko

, p. 807 - 814 (2007/10/02)

Benzothiazolium N-phenacylide, generated in situ from 3-phenacylbenzothiazolium bromide and triethylamine, reacted with maleic anhydride, N-(p-methoxyphenyl)maleimide, dimethyl maleate, and fumarate to give the corresponding tetrahydropyrrolobenzot

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