Cas 215673-99-7,5-<i>tert</i>-butyl-3-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-yl)-7-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-ylmethyl)-3,3a-dihydro-benzo[<i>c</i>]isothiazole

215673-99-7

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Basic information

Product Name: 5-tert-butyl-3-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-yl)-7-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-ylmethyl)-3,3a-dihydro-benzo[c]isothiazole
Synonyms:
CAS NO:215673-99-7
Molecular Formula:
Molecular Weight: 776.141
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: 5-tert-butyl-3-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-yl)-7-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-ylmethyl)-3,3a-dihydro-benzo[c]isothiazole(CAS DataBase Reference)
NIST Chemistry Reference: 5-tert-butyl-3-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-yl)-7-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-ylmethyl)-3,3a-dihydro-benzo[c]isothiazole(215673-99-7)
EPA Substance Registry System: 5-tert-butyl-3-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-yl)-7-(2,6,2'',6''-tetramethyl-[1,1';3',1'']terphenyl-2'-ylmethyl)-3,3a-dihydro-benzo[c]isothiazole(215673-99-7)

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: 215673-99-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 215673-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,6,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 215673-99:
(8*2)+(7*1)+(6*5)+(5*6)+(4*7)+(3*3)+(2*9)+(1*9)=147
147 % 10 = 7
So 215673-99-7 is a valid CAS Registry Number.

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215673-99-7Relevant academic research and scientific papers

Novel intramolecular cyclization reaction involving a thionitroso group: Formation of a 3,3a-dihydro-2,1-benzisothiazole from an o-alkylthionitrosoarene

Tan, Bo,Goto, Kei,Kobayashi, Junji,Okazaki, Renji

, p. 981 - 982 (2007/10/03)

A thionitrosoarene generated by the desulfurization reaction of a stable N-thiosulfinylaniline bearing a bowl-type substituent underwent the intramolecular cyclization reaction involving the ortho-alkyl group to afford the corresponding 3,3a-dihydro-2,1-benzisothiazole. The intermediacy of the thionitrosoarene was corroborated by a trapping experiment with aniline.

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