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1,1':2',1'':3'',1''':2''',1''''-Quinquephenyl, 3',3''',4',4''',5',5''',6',6'''-octaphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193010-58-1

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193010-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193010-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,0,1 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 193010-58:
(8*1)+(7*9)+(6*3)+(5*0)+(4*1)+(3*0)+(2*5)+(1*8)=111
111 % 10 = 1
So 193010-58-1 is a valid CAS Registry Number.

193010-58-1SDS

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-bis(pentaphenylphenyl)benzene

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:193010-58-1 SDS

193010-58-1Downstream Products

193010-58-1Relevant academic research and scientific papers

The albatrossenes: Large, cleft-containing, polyphenyl polycyclic aromatic hydrocarbons

Tong, Ling,Ho, Douglas M.,Vogelaar, Nancy J.,Schutt, Clarence E.,Pascal Jr., Robert A.

, p. 7291 - 7302 (2007/10/03)

The syntheses and X-ray structures of very large polycyclic aromatic compounds containing clefts defined by polyphenylaryl groups are described. The C2-symmetric 'albatrossenes' 1,3-bis(heptaphenyl-2-naphthyl)benzene (7a) and 1,3-bis(heptaphenyl-1-naphthyl)benzene (12a), as well as brominated derivatives, were synthesized by the addition of tetraphenylbenzyne to the appropriate polyphenyl biscyclopentadienones. The 2-naphthyl isomers have wide, shallow clefts, and the 1-naphthyl isomers have deep, narrow clefts which were observed to change size dramatically in different crystal environments. In a similar way, 1,3,5-tris(pentaphenylphenyl)benzene (19), a D3-symmetric molecular propeller with a diameter of 21 ?, and 1,3,5-tris(heptaphenyl-2-naphthyl)benzene (22) were prepared by the addition of diphenylacetylene and tetraphenylbenzyne, respectively, to a triscyclopentadienone.

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