1,8-Diiodooctane(DIO) - ≥96% , CAS No.24772-63-2

CAS: 24772-63-2 Cat. No.: D473785 Summenformel: C₈H₁₆I₂ Molekulargewicht: 366.02 Beilstein Registry Number: 1735440 EG-Nummer: 246-456-6

GRADE & PURITY ≥96%

Synonyms

SY048299 | 1,8-Diiodooctane , stabilized with Copper | 1,8-bis(iodanyl)octane | F19540 | J-015668 | Octane,1,8-diiodo- | FT-0607049 | DTXSID8067020 | A817488 | D2158 | MFCD00001106 | EINECS 246-456-6 | 1,8-Diiodooctane, stabilized with copper | SCHEMBL630

Storage

Room temperature,Argon charged

Shipped In

Normal

Übersicht

Description

1,8-Diiodooctane has been employed as processing additive:to improve the morphology and the efficiency of bulk heterojunctions solar cells, based on the regioregular poly(3-hexylthiophene) and a soluble fullerene derivativeto improve the power conversion efficiency of polymer solar cells

Specifications

Synonyme

SY048299 | 1,8-Diiodooctane , stabilized with Copper | 1,8-bis(iodanyl)octane | F19540 | J-015668 | Octane,1,8-diiodo- | FT-0607049 | DTXSID8067020 | A817488 | D2158 | MFCD00001106 | EINECS 246-456-6 | 1,8-Diiodooctane, stabilized with copper | SCHEMBL630

Spezifikationen & Reinheit

≥96%

Storage

Room temperature,Argon charged

Verschickt in

Normal

Reinheit

≥96%

Namen und Kennungen

• Pubchem Sid: 504756040
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756040
• Kanonisches Lächeln: C(CCCCI)CCCI
• IUPAC Name: 1,8-diiodooctane
• InChIKey: KZDTZHQLABJVLE-UHFFFAOYSA-N
• INCHI: 1S/C8H16I2/c9-7-5-3-1-2-4-6-8-10/h1-8H2
• Isomere SMILES: C(CCCCI)CCCI
• WGK Deutschland: 3
• Molekulargewicht: 366.02
• Beilstein: 1735440
• Reaxy-Rn: 1735437
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1735437&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Klasse Organoiodides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Klasse: Organoiodides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organoiodides
• Alternative Parents: Hydrocarbon derivatives Alkyl iodides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Organoiodide - Alkyl iodide - Alkyl halide - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as organoiodides. These are compounds containing a chemical bond between a carbon atom and an iodine atom.
• External Descriptors: Not available

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

Chemische und physikalische Eigenschaften

• Empfindlichkeit: light sensitive；air sensitive
• Brechungsindex: 1.56
• Flammpunkt (°F): 235.4 °F
• Flammpunkt (°C): 113 °C
• Siedepunkt (°C): 144°C/2mmHg(lit.)
• Molekulargewicht: 366.020 g/mol
• XLogP3: 5.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 7
• Exact Mass: 365.934 Da
• Monoisotopic Mass: 365.934 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 47.200
• 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

Referenzen

1. Xingjuan Ma, Jiaqi Kong, Wei Wang, Xin Li.  (2022)  Green-Solvent Engineering for Depositing Qualified Phenyl-C61-butyl Acid Methyl Ester Films for Inverted Flexible Perovskite Solar Cells.  ACS Applied Materials & Interfaces,      [PMID:36574762] [10.1021/acsami.2c17694]

2. Lanxiang Yu, Hansheng Chen, Chen Xie, Qingqing Zheng, Shuyi Liu, Siyue Zhou, Xuanlin Wen, Baoshen Deng, Mengshi Fang, Shenghua Liu, Hui Liu.  (2026)  Optimized Molecular Nucleation Behaviors in Highly Efficient Organic Solar Cells Enabled by a Bezothiophene-Based Solid Additive.  Polymers,  18  (16): (1939).  [PMID:42655221] [10.3390/polym18161939]