1,2-Dimethylnaphthalene - ≥95% , CAS No.573-98-8

CAS: 573-98-8 Cat. No.: D155010 Formula: C₁₂H₁₂ Peso molecolare: 156.23 Beilstein Registry Number: 2039380 Numero EC: 209-364-7

GRADE & PURITY ≥95%

Synonyms

Q27115775 | 1,2-Dimethylnaphthalene, 98% | Naphthalene, dimethyl- | 1,2-DIMETHYLNAPHTHALENE | 1,2-Dimethyl-naphthalene | 1,2-Dimethylnaphthalene, 95% | BDBM50159280 | DSSTox_CID_5130 | D89712 | FT-0606428 | NSC59832 | NSC-59832 | Tox21_202167 | 23T7O135BD

Storage

Argon charged,Room temperature

Shipped In

Normal

Panoramica

Product Describtion:

1,2-Dimethylnaphthalene is a polycyclic aromatic hydrocarbon. Its effect on the naupliar and adult stages of the marine cyclopoid copepod Oithona davisae is reported.

Product Application:

1,2-Dimethylnaphthalene is suitable reagent used to investigate the secondary organic aerosol (SOA) production via gas-phase photooxidation.

Specifications

Sinonimi

Q27115775 | 1,2-Dimethylnaphthalene, 98% | Naphthalene, dimethyl- | 1,2-DIMETHYLNAPHTHALENE | 1,2-Dimethyl-naphthalene | 1,2-Dimethylnaphthalene, 95% | BDBM50159280 | DSSTox_CID_5130 | D89712 | FT-0606428 | NSC59832 | NSC-59832 | Tox21_202167 | 23T7O135BD

Specifiche e purezza

≥95%

Condizioni di conservazione di stoccaggio

Argon charged,Room temperature

Spedito in

Normal

Purezza

≥95%

Nomi e identificatori

• Pubchem Sid: 504752100
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752100
• Sorrisi canonici: CC1=C(C2=CC=CC=C2C=C1)C
• IUPAC Name: 1,2-dimethylnaphthalene
• InChIKey: QNLZIZAQLLYXTC-UHFFFAOYSA-N
• INCHI: 1S/C12H12/c1-9-7-8-11-5-3-4-6-12(11)10(9)2/h3-8H,1-2H3
• Isomeri SMILES: CC1=C(C2=CC=CC=C2C=C1)C
• WGK Germania: 3
• Peso molecolare: 156.23
• Beilstein: 2039380
• Reaxy-Rn: 2039376
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2039376&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Naphthalenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Naphthalenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Naphthalenes
• Alternative Parents: Aromatic hydrocarbons Polycyclic hydrocarbons Unsaturated hydrocarbons
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Naphthalene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
• External Descriptors: dimethylnaphthalene

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

Obiettivi associati (umani)

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

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

KCNH2 Tclin HERG (29587 Activities)

Discover Target: KCNH2

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

CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

Discover Target: CYP1A2

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

CYP2A6 Tchem Cytochrome P450 2A6 (2861 Activities)

Discover Target: CYP2A6

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

Obiettivi associati (non umani)

Cyp2a5 Cytochrome P450 2A5 (126 Activities)

Discover Target: Cyp2a5

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Difficult to mix in water.
• Sensibilità: Air Sensitive
• Indice di rifrazione: 1.62
• Punto di infiammabilità (°F): 235.4 °F
• Punto di infiammabilità (°C): 113 °C
• Punto di ebollizione (°C): 132°C/12mmHg(lit.)
• Punto di fusione (°C): -2 °C
• Peso molecolare: 156.220 g/mol
• XLogP3: 4.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 156.094 Da
• Monoisotopic Mass: 156.094 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 150.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Riferimenti

1. Tao Sun, Qiuchen Huang, Wei Zhang, Ruonan Chen, Wei Li, Haipeng Chen, Shaoqiang Hu, Zhiqiang Cai.  (2022)  Performance and selectivity of amphiphilic pillar[5]arene as stationary phase for capillary gas chromatography.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:35390736] [10.1016/j.chroma.2022.463008]

2. Xiaohong Yang, Changxia Li, Meiling Qi, Liangti Qu.  (2016)  Graphene-ZIF8 composite material as stationary phase for high-resolution gas chromatographic separations of aliphatic and aromatic isomers.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:27423773] [10.1016/j.chroma.2016.07.029]