Cas 863324-11-2,2-(2-{4,5-dimethoxy-2-[(triisopropylsilanyl)-ethynyl]-phenyl}-ethyl)-isoindole-1,3-dione

863324-11-2

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Basic information

Product Name: 2-(2-{4,5-dimethoxy-2-[(triisopropylsilanyl)-ethynyl]-phenyl}-ethyl)-isoindole-1,3-dione
Synonyms: 2-(2-{4,5-dimethoxy-2-[(triisopropylsilanyl)-ethynyl]-phenyl}-ethyl)-isoindole-1,3-dione
CAS NO:863324-11-2
Molecular Formula:
Molecular Weight: 491.703
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-{4,5-dimethoxy-2-[(triisopropylsilanyl)-ethynyl]-phenyl}-ethyl)-isoindole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2-{4,5-dimethoxy-2-[(triisopropylsilanyl)-ethynyl]-phenyl}-ethyl)-isoindole-1,3-dione(863324-11-2)
EPA Substance Registry System: 2-(2-{4,5-dimethoxy-2-[(triisopropylsilanyl)-ethynyl]-phenyl}-ethyl)-isoindole-1,3-dione(863324-11-2)

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: 863324-11-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 863324-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,3,2 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 863324-11:
(8*8)+(7*6)+(6*3)+(5*3)+(4*2)+(3*4)+(2*1)+(1*1)=162
162 % 10 = 2
So 863324-11-2 is a valid CAS Registry Number.

863324-11-2Upstream product

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863324-11-2Relevant academic research and scientific papers

Construction of the benzindenoazepine skeleton via cyclopentannulation of Fischer aminocarbene complexes: Total synthesis of bulgaramine

Giese, Matthew W.,Moser, William H.

, p. 6222 - 6229 (2007/10/03)

A total synthesis of bulgaramine has been accomplished with a longest linear sequence of eight steps and an overall yield of 23% from commercially available 3,4-dimethoxyphenethyl alcohol. An intramolecular cyclopentannulation reaction of a Fischer aminoc

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