Phthaloyl chloride - ≥98% , CAS No.88-95-9

CAS: 88-95-9 Cat. No.: P106938 Fórmula: C₈H₄Cl₂O₂ Peso molecular: 203.02 Beilstein Registry Number: 608200 Número EC: 201-869-0

GRADE & PURITY ≥98%

Synonyms

PHTHALOYL CHLORIDE | 1,2-Bis(chlorocarbonyl)benzene | STL453643 | 1,2-Phthaloyl dichloride | benzene-1,2-dicarbonyl dichloride | Phthalic acid dichloride | 1,2-Benzenedicarbonyl dichloride | PHTHALOYL CHLORIDE [MI] | CCRIS 8625 | EINECS 201-869-0 | W-1003

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Specifications

Sinónimos

PHTHALOYL CHLORIDE | 1,2-Bis(chlorocarbonyl)benzene | STL453643 | 1,2-Phthaloyl dichloride | benzene-1,2-dicarbonyl dichloride | Phthalic acid dichloride | 1,2-Benzenedicarbonyl dichloride | PHTHALOYL CHLORIDE [MI] | CCRIS 8625 | EINECS 201-869-0 | W-1003

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature,Argon charged

Enviado en

FedEx DG Service

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 528775863
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/528775863
• Sonrisas canónicas: C1=CC=C(C(=C1)C(=O)Cl)C(=O)Cl
• IUPAC Name: benzene-1,2-dicarbonyl chloride
• InChIKey: FYXKZNLBZKRYSS-UHFFFAOYSA-N
• INCHI: 1S/C8H4Cl2O2/c9-7(11)5-3-1-2-4-6(5)8(10)12/h1-4H
• Isómeros SMILES: C1=CC=C(C(=C1)C(=O)Cl)C(=O)Cl
• WGK Alemania: 3
• Número ONU: 3265
• Grupo de embalaje: II
• Peso molecular: 203.02
• Beilstein: 608200
• Reaxy-Rn: 608200
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=608200&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Benzoic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Benzoic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzoic acids and derivatives
• Alternative Parents: Benzoyl derivatives Acyl chlorides Organooxygen compounds Organochlorides Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Benzoic acid or derivatives - Benzoyl - Acyl halide - Acyl chloride - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as benzoic acids and derivatives. These are organic compounds containing a carboxylic acid substituent attached to a benzene ring.
• 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

• Solubilidad: Miscible with ether.
• Sensibilidad: Moisture & Light sensitive ;air sensitive
• Punto de congelación (°C): 12 °C
• Índice de refracción: 1.5692
• Punto de inflamación (°F): 235.4 °F - closed cup
• Punto de inflamación (°C): 113 °C - closed cup
• Punto de ebullición (°C): 269-271 °C (lit.)
• Punto de fusión (°C): 6-12 °C (lit.)
• Peso molecular: 203.020 g/mol
• XLogP3: 2.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 201.959 Da
• Monoisotopic Mass: 201.959 Da
• Topological Polar Surface Area: 34.100 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 181.000
• 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. Zhenghui Yang, Haiquan Guo, Chuanqing Kang, Lianxun Gao.  (2021)  Synthesis and characterization of amide-bridged colorless polyimide films with low CTE and high optical performance for flexible OLED displays.  Polymer Chemistry,  12  (37): (5364-5376).  [PMID:] [10.1039/D1PY00762A]

2. Jin Wang, Wubin Wang, Yufei Yan, Yaxuan Liu, Guangxu Zhang, Jizhen Li, Yuyao Wu.  (2025)  Impact of acyl chloride monomers on the structure and performance of polyamide nanofiltration membranes for lithium-magnesium separation.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2025.123858]

3. Yongchao He, Hanzhao Kuang, Xiaoqing Liu, Hai Zheng, Yinhang Zhang, Xuan Wang, Yinghua Huang, Jinjing Tang, Feng Wang, Xudong Cui, Mingbo Yang, Hang Chen, Yanhao Huang.  (2026)  2D-QSAR-DFT assisted design of unimolecular coumarin oxime ester photoinitiators with terminal fluorobenzene moieties for radical polymerization.  POLYMER,      [PMID:] [10.1016/j.polymer.2026.129738]