1210-35-1 | Dibenzosuberone

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$15.00	$10.00
5g	98%	in stock	$16.00	$11.00
25g	98%	in stock	$29.00	$20.00
100g	98%	in stock	$78.00	$54.00
250g	98%	in stock	$145.00	$102.00
1kg	98%	in stock	$389.00	$272.00
5kg	98%	in stock	$1,658.00	$1,161.00

Description

• Catalog Number: AI13490
• Chemical Name: Dibenzosuberone
• CAS Number: 1210-35-1
• Molecular Formula: C15H12O
• Molecular Weight: 208.25518000000005
• MDL Number: MFCD00003587
• SMILES: O=C1c2ccccc2CCc2c1cccc2
• NSC Number: 49727

Computed Properties

• Complexity: 245
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 4

Upstream Synthesis Route

Dibenzo[a,d]cycloheptadien-5-one, also known as $name$, is a versatile chemical compound frequently utilized in organic synthesis. With its unique structure and reactivity, it plays a crucial role in a variety of chemical reactions and transformations. In chemical synthesis, $name$ serves as a key building block for the construction of intricate organic molecules due to its ability to participate in various types of reactions. Its aromatic ring system provides stability and facilitates the formation of new bonds, making it an essential component in the creation of complex organic frameworks. One of the primary applications of $name$ is in the synthesis of biologically active compounds, pharmaceuticals, and agrochemicals. Its structural features allow for the modification of its chemical properties through functional group transformations, enabling chemists to tailor its reactivity to specific synthetic pathways. Additionally, $name$ can be used as a precursor for the synthesis of natural products and heterocyclic compounds, expanding its utility in organic chemistry.Overall, the versatile nature of Dibenzo[a,d]cycloheptadien-5-one makes it an invaluable tool in chemical synthesis, enabling the efficient creation of diverse organic molecules with a wide range of applications in various industries.

Literature

• Design, synthesis, and biological evaluation of novel disubstituted dibenzosuberones as highly potent and selective inhibitors of p38 mitogen activated protein kinase.

  Journal of medicinal chemistry 20120628

• Evidence for the involvement of the monoaminergic system in the antidepressant-like action of two 4-amine derivatives of 10,11-dihydro-5H-dibenzo [a,d] cycloheptane in mice evaluated in the tail suspension test.

  Progress in neuro-psychopharmacology & biological psychiatry 20080215

• Sensitive extractive spectrophotometric methods for the determination of nortriptyline hydrochloride in pharmaceutical formulations.

  Chemical & pharmaceutical bulletin 20071201

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

• Synthesis of novel, potentially biologically active dibenzosuberone derivatives.

  Molecules (Basel, Switzerland) 20051231

• The control of impurities in amitriptyline hydrochloride using a reversed-phase hybrid stationary phase.

  Pharmeuropa scientific notes 20050801

• 2H NMR and X-ray diffraction studies of methyl rotation in crystals of ortho-methyldibenzocycloalkanones.

  Solid state nuclear magnetic resonance 20050701