Succinyl chloride - ≥95% , CAS No.543-20-4

CAS: 543-20-4 Cat. No.: S108669 Peso molecular: 154.98 Beilstein Registry Number: 507064 Número EC: 208-838-0

GRADE & PURITY ≥95%

Synonyms

BS-43814 | FT-0632355 | AMY4013 | D95385 | BP-13425 | Q27279047 | AKOS000121271 | Succinoyl chloride | AI3-17465 | BRN 0507064 | GDN09V9867 | succinic dichloride | SUCCINYL CHLORIDE | 1,2-Ethanediylbis(chloroformate) | WLN: GV2VG | 1,2-Bis(chlorocarbonyl)

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Specifications

Sinónimos

BS-43814 | FT-0632355 | AMY4013 | D95385 | BP-13425 | Q27279047 | AKOS000121271 | Succinoyl chloride | AI3-17465 | BRN 0507064 | GDN09V9867 | succinic dichloride | SUCCINYL CHLORIDE | 1, 2-Ethanediylbis(chloroformate) | WLN: GV2VG | 1, 2-Bis(chlorocarbonyl)

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

FedEx DG Service

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

Pureza

≥95%

Nombres e identificadores

• Sonrisas canónicas: C(CC(=O)Cl)C(=O)Cl
• IUPAC Name: butanedioyl dichloride
• InChIKey: IRXBNHGNHKNOJI-UHFFFAOYSA-N
• INCHI: 1S/C4H4Cl2O2/c5-3(7)1-2-4(6)8/h1-2H2
• Isómeros SMILES: C(CC(=O)Cl)C(=O)Cl
• WGK Alemania: 3
• RTECS: WN4900000
• Número ONU: 3265
• Grupo de embalaje: II
• Peso molecular: 154.98
• Beilstein: 507064
• Reaxy-Rn: 507064

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Clase Acyl halides
      • Subclass Acyl chlorides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Clase: Acyl halides
• Subclass: Acyl chlorides
• Intermediate Tree Nodes: Not available
• Direct Parent: Acyl chlorides
• Alternative Parents: Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acyl chloride - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as acyl chlorides. These are organic compounds containing the functional group -CO-Cl.
• 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: Reacts violently with water.
• Sensibilidad: Moisture Sensitive；Air sensitive
• Punto de congelación (°C): 14 °C
• Índice de refracción: 1.4660 to 1.4720
• Punto de inflamación (°F): 76℃
• Punto de inflamación (°C): 76℃
• Punto de ebullición (°C): 190°C
• Punto de fusión (°C): 15-18°C
• Peso molecular: 154.980 g/mol
• XLogP3: 1.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 153.959 Da
• Monoisotopic Mass: 153.959 Da
• Topological Polar Surface Area: 34.100 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 96.600
• 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. Lin-Xuan Han, Ze-Yong Zhao, Cong Deng, Yu-Zhong Wang.  (2022)  Piperazine/Alkene-Containing Phosphoramide Oligomer for the Intumescent Flame Retardation of EPDM Rubber.  POLYMER DEGRADATION AND STABILITY,      [PMID:] [10.1016/j.polymdegradstab.2022.109990]

2. Dong-Wei Wang, Shu-Juan Li, Xue-Ying Tan, Jin-Hui Wang, Ying Hu, Zeng Tan, Jing Liang, Jing-Bo Hu, Yan-Guo Li, Yu-Fen Zhao.  (2020)  Engineering of stepwise-targeting chitosan oligosaccharide conjugate for the treatment of acute kidney injury.  CARBOHYDRATE POLYMERS,      [PMID:33483059] [10.1016/j.carbpol.2020.117556]

3. De Bai, Qin Chen, Yang Chai, Tianhua Ren, Caijuan Huang, Ian D. V. Ingram, Michael North, Qiang Zheng, Haibo Xie.  (2018)  Vanillin derived a carbonate dialdehyde and a carbonate diol: novel platform monomers for sustainable polymers synthesis.  RSC Advances,  8  (60): (34297-34303).  [PMID:35548608] [10.1039/C8RA07185C]

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5. Shi-Song Han, Ze-Yong Li, Jing-Yi Zhu, Kai Han, Zheng-Yang Zeng, Wei Hong, Wen-Xin Li, Hui-Zhen Jia, Yun Liu, Ren-Xi Zhuo, Xian-Zheng Zhang.  (2015)  Dual-pH Sensitive Charge-Reversal Polypeptide Micelles for Tumor-Triggered Targeting Uptake and Nuclear Drug Delivery.  Small,  11  (21): (2543-2554).  [PMID:25626995] [10.1002/smll.201402865]

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7. Na Sun, Mei Qu, Mengyu Wang, Yanna Lv, Liuya Wei, Yu Duan.  (2020)  Synthesis, oral bioavailability evaluation and antiplatelet aggregation activity of three derivatives of 3,4‑dihydroxyacetophenone.  INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE,  45  (3): (919-930).  [PMID:31985017] [10.3892/ijmm.2020.4469]