Cas 910052-74-3,trifluoro-methanesulfonic acid 1-(1-phenyl-ethyl)-2,3-dihydro-1<i>H</i>-pyrrolo[2,3-<i>b</i>]pyridin-6-yl ester

910052-74-3

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Basic information

Product Name: trifluoro-methanesulfonic acid 1-(1-phenyl-ethyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-6-yl ester
Synonyms: trifluoro-methanesulfonic acid 1-(1-phenyl-ethyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-6-yl ester
CAS NO:910052-74-3
Molecular Formula:
Molecular Weight: 372.368
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: trifluoro-methanesulfonic acid 1-(1-phenyl-ethyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-6-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: trifluoro-methanesulfonic acid 1-(1-phenyl-ethyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-6-yl ester(910052-74-3)
EPA Substance Registry System: trifluoro-methanesulfonic acid 1-(1-phenyl-ethyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-6-yl ester(910052-74-3)

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: 910052-74-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 910052-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,0,5 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 910052-74:
(8*9)+(7*1)+(6*0)+(5*0)+(4*5)+(3*2)+(2*7)+(1*4)=123
123 % 10 = 3
So 910052-74-3 is a valid CAS Registry Number.

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910052-74-3Relevant academic research and scientific papers

Synthesis and cross-coupling reactions of 7-azaindoles via a new donor-acceptor cyclopropane

Zheng, Xiaomei,Kerr, Michael A.

, p. 3777 - 3779 (2006)

A new type of donor-acceptor cyclopropane has been prepared from commercially available cyclopropane-1,1-diesters. This cyclopropane reacts with triflic anhydride to produce an isolable tristrifloxy intermediate which when treated with primary amines give

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