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5,7-diphenyl-1,3-diazatricyclo[3.3.1.1~3,7~]decane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38705-08-7

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38705-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38705-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,0 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38705-08:
(7*3)+(6*8)+(5*7)+(4*0)+(3*5)+(2*0)+(1*8)=127
127 % 10 = 7
So 38705-08-7 is a valid CAS Registry Number.

38705-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Diazatricyclo(3.3.1.13,7)decane, 5,7-diphenyl-

1.2 Other means of identification

Product number -
Other names 5,7-diphenyl-1,3-diaza-adamantane

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:38705-08-7 SDS

38705-08-7Relevant academic research and scientific papers

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.

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