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8H-Indeno[2,1-b]phenanthrene is a polycyclic aromatic hydrocarbon (PAH) consisting of three fused benzene rings and a five-membered ring, with the molecular formula C21H14. It is a colorless solid with a melting point of 230-232°C. 8H-Indeno[2,1-b]phenanthrene is known for its potential environmental and health impacts, as PAHs are considered carcinogenic and can be released into the environment through incomplete combustion of organic materials. 8H-Indeno[2,1-b]phenanthrene is also used as a research chemical and in the synthesis of other compounds. Due to its complex structure and potential hazards, it is important to handle this chemical with care and proper safety measures.

241-28-1

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241-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 241-28-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,4 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 241-28:
(5*2)+(4*4)+(3*1)+(2*2)+(1*8)=41
41 % 10 = 1
So 241-28-1 is a valid CAS Registry Number.

241-28-1Downstream Products

241-28-1Relevant academic research and scientific papers

Cycloaromatization of α-oxoketene dithioacetals and β-oxodithioacetals with benzyl-,1-(naphthylmethyl) and 2-(naphthylmethyl)magnesium halides: Synthesis of condensed polynuclear aromatic hydrocarbons

Srinivasa Rao,Balu, Maliakel P.,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar

, p. 3499 - 3510 (2007/10/02)

An efficient route for the synthesis of substituted naphthalenes, phenanthrenes and other polynuclear aromatic hydrocarbons has been developed. The methodology involves 1,2- (or sequential 1,4- and 1,2-) addition of either benzyl, 1-(naphthylmethyl) or 2-(naphthylmethyl) magnesium halides to α-oxoketene dithioacetals or β-oxodithioacetals followed by borontrifluoride etherate catalyzed cycloaromatization of the resulting carbinols.

Synthesis of Oxygenated Metabolites of Indenopyrene

Rice, Joseph E.,LaVoie, Edmond J.

, p. 2428 - 2434 (2007/10/02)

The syntheses of cis- and trans-1,2-dihydro-1,2-dihydroxyindenopyrene, 1,2-dihydroindenopyrene 1,2-epoxide, and 1-, 2-, 6-, 7-, 8-, 9-, and 10-hydroxyindenopyrene are described.UV and high-resolution NMR spectral data are rep

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