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(4bR,10aS)-4-methoxy-4b,10,10a-trimethyl-4b,5,10,10a-tetrahydro-11H-10,5-(epoxymethano)benzo[b]fluorene-11,13-dione is a synthetic organic compound characterized by its complex molecular structure. It is a dione, which means it contains two carbonyl groups, and it also has a methoxy group. (4bR,10aS)-4-methoxy-4b,10,10a-trimethyl-4b,5,10,10a-tetrahydro-11H-10,5-(epoxymethano)benzo[b]fluorene-11,13-dione is a derivative of benzo[b]fluorene, a polycyclic aromatic hydrocarbon. Its stereochemistry is defined by the (4bR,10aS) designation, which specifies the configuration of its chiral centers. (4bR,10aS)-4-methoxy-4b,10,10a-trimethyl-4b,5,10,10a-tetrahydro-11H-10,5-(epoxymethano)benzo[b]fluorene-11,13-dione holds potential applications in medicinal chemistry and material science, and its intricate structure makes it a subject of interest in organic synthesis and chemical research.

85749-68-4

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85749-68-4 Usage

Uses

Used in Medicinal Chemistry:
(4bR,10aS)-4-methoxy-4b,10,10a-trimethyl-4b,5,10,10a-tetrahydro-11H-10,5-(epoxymethano)benzo[b]fluorene-11,13-dione is used as a compound in medicinal chemistry for its potential to be developed into pharmaceutical agents. Its unique structure and functional groups may offer novel therapeutic properties, making it a candidate for further research and development in drug discovery.
Used in Material Science:
In the field of material science, (4bR,10aS)-4-methoxy-4b,10,10a-trimethyl-4b,5,10,10a-tetrahydro-11H-10,5-(epoxymethano)benzo[b]fluorene-11,13-dione is used to explore its potential in creating new materials with specific properties. Its complex structure and chemical composition could contribute to the development of advanced materials for various applications, such as in electronics, coatings, or other high-tech industries.
Used in Organic Synthesis:
(4bR,10aS)-4-methoxy-4b,10,10a-trimethyl-4b,5,10,10a-tetrahydro-11H-10,5-(epoxymethano)benzo[b]fluorene-11,13-dione is utilized in organic synthesis as a starting material or intermediate for the synthesis of other complex organic compounds. Its unique structure and reactivity can be leveraged to create new molecules with potential applications in various fields.
Used in Chemical Research:
In chemical research, (4bR,10aS)-4-methoxy-4b,10,10a-trimethyl-4b,5,10,10a-tetrahydro-11H-10,5-(epoxymethano)benzo[b]fluorene-11,13-dione serves as a subject of study to understand the properties and reactions of complex organic molecules. Its synthesis and manipulation can provide insights into new chemical reactions and mechanisms, contributing to the advancement of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 85749-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,4 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85749-68:
(7*8)+(6*5)+(5*7)+(4*4)+(3*9)+(2*6)+(1*8)=184
184 % 10 = 4
So 85749-68-4 is a valid CAS Registry Number.

85749-68-4SDS

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 NSC377530

1.2 Other means of identification

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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

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More Details:85749-68-4 SDS

85749-68-4Downstream Products

85749-68-4Relevant academic research and scientific papers

Thermolysis of Benzopyranone-Idenone Adducts. 2. Some New Aspects of the Mechanism

Vanderzande, Dirk J.,Kiekens, Eric G.,Martens Henri J.,Hoornaert, Georges J.

, p. 1019 - 1025 (2007/10/02)

Thermolysis of benzopyranone-indenone adducts 1, probably proceeding via o-quinodimethanes 10, gives C-nor-D-homo steroids 4, benzofluorenones 5, and traces of benzocyclopropafluorenones 6.Evidence is presented for the intervention of a biradica

Thermolysis of Benzopyranone-Indenone Adducts: A New Route to the C-Nor-D-Homo Steroid Skeleton

Vanderzande, Dirk J.,Ceustermans, Roger A.,Martens, Henri J.,Toppet, Suzanne M.,Hoornaert, Georges J.

, p. 2188 - 2193 (2007/10/02)

Generation of o-quinodimethane systems and their rearrangement reactions during thermolysis of benzopyranone-indenone adducts 9 have been studied.Three products have been obtained: a C-nor-D-homo steroid, 12, a benzofluorenone, 13, and a benzocyclop

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