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

CAS: 77-73-6 Cat. No.: D110864 Formule: C₁₀H₁₂ Poids moléculaire: 132.2 Beilstein Registry Number: 1904092 Numéro 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

Vue d’ensemble

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

Synonymes

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

Spécifications et pureté

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

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

FedEx DG Service

Pureté

≥96%

Noms et identifiants

Pubchem Sid

508812276

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508812276

Sourires canoniques

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

Isomères SMILES

C1C=CC2C1C3CC2C=C3

WGK Allemagne

2

RTECS

PC1050000

CAS alternatif

542-92-7

Numéro ONU

2048

Groupe d'emballage

III

Poids moléculaire

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
• Description: 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

Cibles associées (humaines)

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

Cibles associées (non humaines)

Plasmodium falciparum (966862 Activities)

Explore this target

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

Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Immiscible with water.
• Sensibilité: heat sensitive
• Indice de réfraction: 1.51-1.512
• Point d'éclair (°C): 44 °C
• Point d'ébullition (°C): 170°C
• Point de fusion (°C): 32 °C
• Poids moléculaire: 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

Foire aux questions

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.