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1,3-Diazabicyclo[2.2.0]hex-5-en-2-one, 3,4,6-triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75397-89-6

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75397-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75397-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,9 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75397-89:
(7*7)+(6*5)+(5*3)+(4*9)+(3*7)+(2*8)+(1*9)=176
176 % 10 = 6
So 75397-89-6 is a valid CAS Registry Number.

75397-89-6SDS

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 3,4,6-triphenyl-1,3-diazabicyclo[2.2.0]hex-5-en-2-one

1.2 Other means of identification

Product number -
Other names 3,4,6-triphenyl-1,3-diazabicyclo<2.2.0>hex-5-en-2-one

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:75397-89-6 SDS

75397-89-6Downstream Products

75397-89-6Relevant academic research and scientific papers

Novel Synthesis of 2,4-Diarylquinolines by Photochemical followed by Thermal Transformations of 1,4,6-Triarylpyrimidin-2(1H)-ones

Nishio, Takehiko,Omote, Yoshimori

, p. 1773 - 1775 (2007/10/02)

The 2,4-diarylquinolines (3) were obtained in a one-pot synthesis by photochemical and subsequent thermal reactions of 1,4,6-triarylpyrimidin-2(1H)-ones (1) in fair yield.The quinolines (3) were formed via thermal cycloreversion, followed by electrocyclic ring-closure, of the 1,3-diazabicyclohex-5-en-2-ones (2), which were produced by photochemical electrocyclization of the pyrimidin-2(1H)-ones (1).

NOVEL SYNTHESIS OF 2,4-DIPHENYLQUINOLINES

Nishio, Takehiko,Katahira, Katsuhiro,Omote, Yoshimori

, p. 2825 - 2826 (2007/10/02)

2,4-Diphenylquinolines (3) were quantitatively prepared by heating of 3-aryl-4,6-diphenyl-2-oxo-1,3-diazabicyclohex-5-enes (2), which were obtained by photochemical electrocyclization of 1-aryl-4,6-diphenyl-2(1H)-pyrimidin-2-ones (1), in benzene at reflux temperature.

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