N,n'-hexamethylenebisacrylamide - ≥98% , CAS No.7150-41-6

CAS: 7150-41-6 Cat. No.: N304466 Peso molecular: 224.299 Número EC: 801-251-6

GRADE & PURITY ≥98%

Synonyms

7150-41-6|N-[6-(prop-2-enoylamino)hexyl]prop-2-enamide|N,N-HEXAMETHYLENEBISACRYLAMIDE|1,6-Hexamethylenebisacrylamide|n,n'-hexamethylene-bis-acrylamide|N,N'-HEXAMETHYLENEBISACRYLAMIDE|NSC70085|SCHEMBL58169|YSZC266|n,n'-hexamethylene bisacrylamide|DTXSID609

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

7150-41-6 | N-[6-(prop-2-enoylamino)hexyl]prop-2-enamide | N, N-HEXAMETHYLENEBISACRYLAMIDE | 1, 6-Hexamethylenebisacrylamide | n, n'-hexamethylene-bis-acrylamide | N, N'-HEXAMETHYLENEBISACRYLAMIDE | NSC70085 | SCHEMBL58169 | YSZC266 | n, n'-hexamethylene bisacrylamide | DTXSID609

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

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

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504758105
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504758105
• Sonrisas canónicas: C=CC(=O)NCCCCCCNC(=O)C=C
• IUPAC Name: N-[6-(prop-2-enoylamino)hexyl]prop-2-enamide
• InChIKey: YQCFXPARMSSRRK-UHFFFAOYSA-N
• INCHI: 1S/C12H20N2O2/c1-3-11(15)13-9-7-5-6-8-10-14-12(16)4-2/h3-4H,1-2,5-10H2,(H,13,15)(H,14,16)
• Isómeros SMILES: C=CC(=O)NCCCCCCNC(=O)C=C
• Peso molecular: 224.299
• Reaxy-Rn: 1783822
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1783822&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Acrylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Acrylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Acrylic acids and derivatives
• Alternative Parents: Secondary carboxylic acid amides Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acrylic acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as acrylic acids and derivatives. These are organic compounds containing acrylic acid CH2=CHCO2H or a derivative thereof.
• 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

• Punto de inflamación (°C): 194.9℃
• Punto de ebullición (°C): 481.5℃ at 760 mmHg
• Peso molecular: 224.300 g/mol
• XLogP3: 1.500
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 9
• Exact Mass: 224.152 Da
• Monoisotopic Mass: 224.152 Da
• Topological Polar Surface Area: 58.200 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 223.000
• 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. Ning Liu, Weina Jia, Xia Li, Xuefeng Yan, Liangmin Yu.  (2023)  A high mechanical strength, deformable, fatigue-resistant polyacrylonitrile nanosphere-reinforced gel electrolyte for supercapacitors.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.145701]

2. Xu Huan, Yi Chen, Xiaozhen Wu, Hui Wang, Ying Yang, Pengkai Wu, Tianqing Liu, Kaikai Wang, Dan Ding.  (2023)  Balancing and Therapeutic Roles of CXCR4-inhibiting Nanomedicine via Synergetic Regulation of Hepatic Stellate Cells and Extracellular Matrix in Liver injury.  CHINESE JOURNAL OF CHEMISTRY,      [PMID:] [10.1002/cjoc.202300217]