Cas 89877-00-9,2,4,6-Trimethyl-benzenesulfonate2-amino-3-phenylethynyl-isoquinolinium;

89877-00-9

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Basic information

Product Name: 2,4,6-Trimethyl-benzenesulfonate2-amino-3-phenylethynyl-isoquinolinium;
Synonyms: 2,4,6-Trimethyl-benzenesulfonate2-amino-3-phenylethynyl-isoquinolinium;
CAS NO:89877-00-9
Molecular Formula:
Molecular Weight: 444.554
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: 2,4,6-Trimethyl-benzenesulfonate2-amino-3-phenylethynyl-isoquinolinium;(CAS DataBase Reference)
NIST Chemistry Reference: 2,4,6-Trimethyl-benzenesulfonate2-amino-3-phenylethynyl-isoquinolinium;(89877-00-9)
EPA Substance Registry System: 2,4,6-Trimethyl-benzenesulfonate2-amino-3-phenylethynyl-isoquinolinium;(89877-00-9)

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: 89877-00-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89877-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,7 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89877-00:
(7*8)+(6*9)+(5*8)+(4*7)+(3*7)+(2*0)+(1*0)=199
199 % 10 = 9
So 89877-00-9 is a valid CAS Registry Number.

89877-00-9Upstream product

89877-00-9Downstream Products

89877-07-6 2-Phenyl-pyrazolo[1,5-b]isoquinoline

89877-00-9Relevant academic research and scientific papers

Thermal Rearrangements of Cyclic Amine Ylides. III. Intramolecular Cyclization of 2-Ethynylpyridine N-Imides to 3-Azaindolizine Derivatives

Tsuchiya, Takashi,Sashida, Haruki,Konoshita, Ari

, p. 4568 - 4572 (2007/10/02)

Treatment of the N-aminopyridinium salts (5a-e) prepared from 2-ethynylpyridines (4) with potassium carbonate resulted in an intramolecular cyclization to give the corresponding 3-azaindolizines (6) (pyrazolopyridines), presumably via the ionic in

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