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(11R,12R)-11,12-dihydronaphtho[1,2,3,4-pqr]tetraphene-11,12-diol, also known as rac-(11R,12R)-11,12-dihydronaphtho[1,2,3,4-pqr]tetraphene-11,12-diol, is a complex chemical compound characterized by a naphthalene backbone with two hydroxyl (OH) groups at positions 11 and 12. This molecule is highly symmetrical and rigid due to its extended structure, making it a valuable reagent or intermediate in organic chemistry for the synthesis of other organic compounds. Its unique structure and properties also suggest potential applications in materials science, pharmaceuticals, and other fields, although its complex nature presents challenges in synthesis and study that require specialized techniques and expertise in organic synthesis and characterization.

153857-27-3

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153857-27-3 Usage

Uses

Used in Organic Chemistry:
(11R,12R)-11,12-dihydronaphtho[1,2,3,4-pqr]tetraphene-11,12-diol is used as a reagent or intermediate for the synthesis of other organic compounds, leveraging its unique structure and properties to facilitate various chemical reactions and the creation of new molecules.
Used in Materials Science:
In the field of materials science, (11R,12R)-11,12-dihydronaphtho[1,2,3,4-pqr]tetraphene-11,12-diol is utilized for its potential to contribute to the development of new materials with specific properties, such as rigidity and symmetry, which can be advantageous in various applications.
Used in Pharmaceutical Industry:
(11R,12R)-11,12-dihydronaphtho[1,2,3,4-pqr]tetraphene-11,12-diol is employed in the pharmaceutical industry for its potential role in the development of new drugs, given its unique chemical structure that may offer novel therapeutic opportunities and mechanisms of action.
Used in Research and Development:
Due to the challenges associated with its synthesis and study, (11R,12R)-11,12-dihydronaphtho[1,2,3,4-pqr]tetraphene-11,12-diol is also used in research and development settings, where chemists and material scientists work to understand its properties and explore new methods for its synthesis and application.

Check Digit Verification of cas no

The CAS Registry Mumber 153857-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,8,5 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 153857-27:
(8*1)+(7*5)+(6*3)+(5*8)+(4*5)+(3*7)+(2*2)+(1*7)=153
153 % 10 = 3
So 153857-27-3 is a valid CAS Registry Number.

153857-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Dibenzo[def,p]chrysene-11,12-diol,11,12-dihydro-,(11R,12R)-rel

1.2 Other means of identification

Product number -
Other names Trans-11,12-dihydroxy-11,12-dihydrodibenzo(a,l)pyrene

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:153857-27-3 SDS

153857-27-3Downstream Products

153857-27-3Relevant academic research and scientific papers

Syntheses of oxidized metabolites implicated as active forms of the highly potent carcinogenic hydrocarbon dibenzo[def,p]chrysene

Zhang,Harvey

, p. 625 - 636 (2007/10/03)

Polycyclic aromatic hydrocarbons (PAHs) are an important class of environmental carcinogens, and dibenzo[def,p]chrysene is the most potent carcinogenic PAH currently known. Syntheses of various oxidized metabolites of dibenzo[def,p]chrysene implicated as the biologically active forms that interact directly or indirectly with DNA to induce mutations that lead to tumor induction are reported. These include the 8,9- and 11,12-dihydrodiols (2 and 3), the 8,9,11,12-bis-dihydrodiol (5), and the fjord region anti-diol epoxide derivative of 3 (4).

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