Dicyclopentadiene(DCPD) - ≥96%, Mixture of isomers,contains 0.03% BHT as stabilizer , CAS No.77-73-6

CAS: 77-73-6 Cat. No.: D110864 Fórmula: C₁₀H₁₂ Peso molecular: 132.2 Beilstein Registry Number: 1904092 Número CE: 201-052-9

GRADE & PURITY ≥96%, Mixture of isomers,contains 0.03% BHT as stabilizer

Synonyms

MLS001055376 | 2-05-00-00391 (Beilstein Handbook Reference) | D0443 | Dicyclopentadiene contains BHT as stabilizer | Biscyclopentadiene | Prometa XP 100 | (3a.alpha.,4.alpha.,7.alpha.,7a.alpha.)-3a,4,7,7a-Tetrahydro-4,7-methano-1H-indene | NCGC00090776-03

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Visão geral

Dicyclopentadiene is used in the preparation of poly(ionic liquid) brushes, used in anti-bacterial and anti-biofouling applications. Also used in the preparation of copolymer structures in the synthesis of nanocapsules.

Specifications

Sinónimos

MLS001055376 | 2-05-00-00391 (Beilstein Handbook Reference) | D0443 | Dicyclopentadiene contains BHT as stabilizer | Biscyclopentadiene | Prometa XP 100 | (3a.alpha.,4.alpha.,7.alpha.,7a.alpha.)-3a,4,7,7a-Tetrahydro-4,7-methano-1H-indene | NCGC00090776-03

Especificações e pureza

≥96%, Mixture of isomers,contains 0.03% BHT as stabilizer

Condições de armazenamento de armazenamento

Room temperature,Argon charged

Enviado em

FedEx DG Service

Pureza

≥96%

Nomes e identificadores

• Pubchem Sid: 508812276
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508812276
• Sorrisos canónicos: C1C=CC2C1C3CC2C=C3
• IUPAC Name: tricyclo[5.2.1.02,6]deca-3,8-diene
• InChIKey: HECLRDQVFMWTQS-UHFFFAOYSA-N
• INCHI: 1S/C10H12/c1-2-9-7-4-5-8(6-7)10(9)3-1/h1-2,4-5,7-10H,3,6H2
• SMILES isoméricas: C1C=CC2C1C3CC2C=C3
• WGK Alemanha: 2
• RTECS: PC1050000
• CAS alternativo: 542-92-7
• Número UN: 2048
• Grupo de embalagem: III
• Peso molecular: 132.2
• Beilstein: 1904092
• Reaxy-Rn: 1904092
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1904092&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Hydrocarbons
    • Classe Polycyclic hydrocarbons

• Kingdom: Organic compounds
• Superclass: Hydrocarbons
• Classe: Polycyclic hydrocarbons
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Polycyclic hydrocarbons
• Alternative Parents: Cyclic olefins Unsaturated aliphatic hydrocarbons
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Polycyclic hydrocarbon - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Olefin - Aliphatic homopolycyclic compound
• Descrição: This compound belongs to the class of organic compounds known as polycyclic hydrocarbons. These are polycyclic organic compounds made up only of carbon and hydrogen atoms.
• External Descriptors: cyclic olefin

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Alvos associados (humanos)

PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)

Discover Target: PPARG

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTH1R Tclin Parathyroid hormone receptor (47172 Activities)

Discover Target: PTH1R

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Lymphoblastoid cell (5959 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Alvos associados (não humanos)

Plasmodium falciparum (966862 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de ação

Propriedades químicas e físicas

• Solubilidade: Immiscible with water.
• Sensibilidade: heat sensitive
• Índice de refração: 1.51-1.512
• Ponto de inflamação (°C): 44 °C
• Ponto de ebulição (°C): 170°C
• Ponto de fusão (°C): 32 °C
• Peso molecular: 132.200 g/mol
• XLogP3: 2.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 132.094 Da
• Monoisotopic Mass: 132.094 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 212.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 4
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Perguntas frequentes

What is the purity of this product?

This product is supplied at ≥96% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.