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112547-35-0

112547-35-0

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112547-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112547-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,5,4 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112547-35:
(8*1)+(7*1)+(6*2)+(5*5)+(4*4)+(3*7)+(2*3)+(1*5)=100
100 % 10 = 0
So 112547-35-0 is a valid CAS Registry Number.

112547-35-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-3,3-dimethyl-2-methylen-2,3-dihydrofuro[3,2-c]chinolin-4-on

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112547-35-0 SDS

112547-35-0Downstream Products

112547-35-0Relevant articles and documents

Acetylenchemie. 4 Mitt. Synthese von Haplophyllin und N-Methylflindersin, zwei Wege zu N-funktionalisierten Pyranochinolin-Alkaloiden

Reisch, Johannes,Bathe, Andreas,Rosenthal, Bernd H. W.,Salehi-Artimani, Reza A.

, p. 869 - 872 (2007/10/02)

Pyranochinolin-Alkaloide (3), geeignete Vorstufen fuer photobiomimetische Dimerisierungen, sind durch PTC-Reaktion eines 4-Hydroxychinolin-2-ons (1) mit 3-Chlor-3-methylbut-1-in zugaenglich, wobei als Nebenprodukt die Furochinolin-2-on-isomere (5) anfallen.Bei der Synthese von Flindersin (3a) wurde zusaetzlich das Oxazolochinolin-5-on (4) gewonnen; bei der vom N-Methylflindersin (3b) das Bis-(N-methyl-4'-hydroxychinolin-2'-on-3'-yl)-isopenten (7).Alkaloiddimere, deren Bildung aus Intermediaten formulierbar ist, traten nicht auf.Die Entstehung von7 bestaetigt bislang diskutierte Reaktionsablaeufe.Haplophyllin (3c) wurde durch N-Alkylierung von 3a mit 3-Methylcrotonsaeurechlormethylester erstmalig synthetisch dargestellt.

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