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anti-<2,2>-transoid-(1,3)-naphthalenophane-1,11-diene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80664-96-6

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80664-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80664-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,6 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80664-96:
(7*8)+(6*0)+(5*6)+(4*6)+(3*4)+(2*9)+(1*6)=146
146 % 10 = 6
So 80664-96-6 is a valid CAS Registry Number.

80664-96-6SDS

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 anti-[2,2]-transoid-(1,3)-naphthalenophane-1,11-diene

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:80664-96-6 SDS

80664-96-6Downstream Products

80664-96-6Relevant academic research and scientific papers

Toward the Understanding of Benzannelated Annulenes: Synthesis and Properties of an - and -Ring Dibenzannelated Dihydropyrenes

Mitchell, Reginald H.,Williams, Richard Vaughan,Dingle, Thomas W.

, p. 2560 - 2571 (1982)

The dibenzannelated - and dihydropyrenes 5 and 7 and dimethyldihydropyrenes 4 and 6 were synthesized from 1,3-bis- and pyrene.The dimethyldihydropyrenes 4 and 6 are relatively stable and their diatropicities are discussed in relation to each other and to other benzannulenes in terms of Kekule structures and bond order calculations.It is shown that transoid fusion of the benzene rings on the annulene only somewhat perturbs the diatropicity of the annulene, whereas cisoid fusion strongly localizes the annulene macroring.Annulenes such as 6 which have transoid-fused benzenoid rings are also shown to display radicaloid properties.

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