Cas 1198108-63-2,5-tert-butyl-13-(3-oxo-1,3-dihydroisobenzofuran-1-yl)-8,16-dimethyl[2.2]metacyclophane

1198108-63-2

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Basic information

Product Name: 5-tert-butyl-13-(3-oxo-1,3-dihydroisobenzofuran-1-yl)-8,16-dimethyl[2.2]metacyclophane
Synonyms:
CAS NO:1198108-63-2
Molecular Formula:
Molecular Weight: 424.583
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-13-(3-oxo-1,3-dihydroisobenzofuran-1-yl)-8,16-dimethyl[2.2]metacyclophane(CAS DataBase Reference)
NIST Chemistry Reference: 5-tert-butyl-13-(3-oxo-1,3-dihydroisobenzofuran-1-yl)-8,16-dimethyl[2.2]metacyclophane(1198108-63-2)
EPA Substance Registry System: 5-tert-butyl-13-(3-oxo-1,3-dihydroisobenzofuran-1-yl)-8,16-dimethyl[2.2]metacyclophane(1198108-63-2)

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: 1198108-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1198108-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,1,0 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1198108-63:
(9*1)+(8*1)+(7*9)+(6*8)+(5*1)+(4*0)+(3*8)+(2*6)+(1*3)=172
172 % 10 = 2
So 1198108-63-2 is a valid CAS Registry Number.

1198108-63-2Upstream product

1198108-60-9 13-tert-butyl-5-[(2-carboxyl)benzoyl]-8,16-dimethyl[2.2]metacylophane

1198108-63-2Downstream Products

1198108-63-2Relevant academic research and scientific papers

Ipso-Acylation of 5, 13-di-tert-butyl-8, 16-dimethyl[2.2]metacyclophane with acid anhydrides: Through-space electronic interaction among the two benzene rings

Shimizu, Tomoe,Paudel, Arjun,Yamato, Takehiko

experimental part, p. 298 - 301 (2009/12/03)

Acylation of 5, 13-di-tert-butyl-8, 16-dimethyl[2.2]metacyclophane with acid anhydrides led to mono-ipso-acylation at the tert-butyl group to give 5-acyl-13-tert-butyl-8, 16-dimethyl[2.2]metacyclophanes, from which the second electrophilic substitition wi

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