2,5-Dibromothieno[3,2-b]thiophene - ≥98% , CAS No.25121-87-3

CAS: 25121-87-3 Cat. No.: D119994 Peso molecular: 298.02 Beilstein Registry Number: 19(4)188 Número EC: 687-363-4

GRADE & PURITY ≥98%

Synonyms

FT-0685617 | BBL102895 | DS-1531 | A5096 | AM20090292 | STL556704 | SCHEMBL144144 | SY033489 | AB93054 | APDAUBNBDJUQGW-UHFFFAOYSA-N | 2,5-DIBROMO-THIENO[3,2-B]THIOPHENE | 2,5-Dibromothieno[3,2-b]thiophene | W-202054 | D3678 | 2,5-Dibromothieno[3,2-b]thio

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Specifications

Sinónimos

FT-0685617 | BBL102895 | DS-1531 | A5096 | AM20090292 | STL556704 | SCHEMBL144144 | SY033489 | AB93054 | APDAUBNBDJUQGW-UHFFFAOYSA-N | 2, 5-DIBROMO-THIENO[3, 2-B]THIOPHENE | 2, 5-Dibromothieno[3, 2-b]thiophene | W-202054 | D3678 | 2, 5-Dibromothieno[3, 2-b]thio

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Protected from light, Store at -20°C, Argon charged

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Sonrisas canónicas: C1=C(SC2=C1SC(=C2)Br)Br
• IUPAC Name: 2,5-dibromothieno[3,2-b]thiophene
• InChIKey: APDAUBNBDJUQGW-UHFFFAOYSA-N
• INCHI: 1S/C6H2Br2S2/c7-5-1-3-4(10-5)2-6(8)9-3/h1-2H
• Isómeros SMILES: C1=C(SC2=C1SC(=C2)Br)Br
• WGK Alemania: 3
• Peso molecular: 298.02
• Beilstein: 19(4)188
• Reaxy-Rn: 129992
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=129992&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Thienothiophenes

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Thienothiophenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Thienothiophenes
• Alternative Parents: 2,3,5-trisubstituted thiophenes Aryl bromides Heteroaromatic compounds Organobromides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Thienothiophene - 2,3,5-trisubstituted thiophene - Aryl halide - Aryl bromide - Heteroaromatic compound - Thiophene - Hydrocarbon derivative - Organobromide - Organohalogen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as thienothiophenes. These are organic compounds containing two thiophene rings fused to each other.
• 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

Propiedades químicas y físicas

• Sensibilidad: Light Sensitive,Air Sensitive,Heat Sensitive
• Punto de fusión (°C): 130°C
• Peso molecular: 298.000 g/mol
• XLogP3: 4.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 297.794 Da
• Monoisotopic Mass: 295.796 Da
• Topological Polar Surface Area: 56.500 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 126.000
• 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

Referencias

1. Lanlan Shen, Zhiru Bai, Yu Jiang, Liying Li, Fengxing Jiang, Jingkun Xu, Huanhuan Qiu, Huixuan Liu, Rongri Tan.  (2023)  Electrosynthesis and Spectroelectrochemistry Properties of Copolymers Based on 3,4-Ethylenedioxythiophene and Quaterthiophenen Derivatives.  International Journal of Electrochemical Science,      [PMID:] [10.20964/2020.09.73]