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19066-35-4

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19066-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19066-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,6 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19066-35:
(7*1)+(6*9)+(5*0)+(4*6)+(3*6)+(2*3)+(1*5)=114
114 % 10 = 4
So 19066-35-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H20N2O/c23-18-20(17-9-5-2-6-10-17)11-19(16-7-3-1-4-8-16)12-21(14-20)15-22(18)13-19/h1-10H,11-15H2

19066-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-diphenyl-1,3-diazatricyclo[3.3.1.13,7]decan-6-one

1.2 Other means of identification

Product number -
Other names 1,3-Diaza-5,7-diphenyl-adamantan-6-on

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:19066-35-4 SDS

19066-35-4Relevant articles and documents

Anti-neoplastic activity of 1,3-diaza-2-functionalized-adamantan-6-one compounds against melanoma cells

Sharabi-Ronen, Yifat,Levinger, Shlomo,Lellouche, Miri Ben-Dahan,Albeck, Amnon

, p. 27 - 37 (2014/01/17)

Four series of 1,3-diaza-2-functionalized-adamantan-6-one derivatives, bearing at the 2 position SO, SO2, POCl and PO2H functional groups, were synthesized via a key quadruple Mannich reaction, followed by transformation of an aminal functionality into th

Synthesis of novel diazabicycles and their antiprotozoal activities

Wolkinger, Volker,Weis, Robert,Belaj, Ferdinand,Kaiser, Marcel,Brun, Reto,Saf, Robert,Seebacher, Werner

body text, p. 1166 - 1172 (2010/03/04)

We describe the synthesis of new diaryl substituted diazabicyclo[3.2.1] octanes from diazepanes which were prepared by the reduction of diazepanones. The formation of the bicyclic system was optimized by microwave irradiation and the structures of the new compounds were established by single crystal structure analysis and NMR spectroscopy. All new compounds were tested for their potencies against Plasmodium falciparum K1 and Trypanosoma b. rhodesiense, the causative organisms of malaria tropica and the East African form of sleeping sickness. CSIRO 2009.

Conformational Control in the 3,7-Diazabicyclononane System

McCabe, P. H.,Milne, N. J.,Sim, G. A.

, p. 625 - 626 (2007/10/02)

The twin-chair or boat-chair conformation of 3,7-diazabicyclononanes can be selected by forming N,N'-derivatives in which the N atoms have planar or pyramidal bonding patterns, respectively, e.g., acyl substituents for the former and arylsulphonyl

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