[3-(Trimethoxysilyl)propyl]succinic Anhydride - ≥95% , CAS No.156088-53-8

CAS: 156088-53-8 Cat. No.: T162303 Peso molecular: 262.33 Número EC: 834-002-5 PubChem CID: 11507216

GRADE & PURITY ≥95%

Synonyms

AKOS037646610 | ZADOWCXTUZWAKL-UHFFFAOYSA-N | MFCD30475663 | D95261 | AS-69765 | 2,5-Furandione, dihydro-3-[3-(trimethoxysilyl)propyl]- | SCHEMBL190737 | 3-(3-trimethoxysilylpropyl)oxolane-2,5-dione | trimethoxysilylpropyl succinic anhydride | 3-trimethox

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Specifications

Sinónimos

AKOS037646610 | ZADOWCXTUZWAKL-UHFFFAOYSA-N | MFCD30475663 | D95261 | AS-69765 | 2, 5-Furandione, dihydro-3-[3-(trimethoxysilyl)propyl]- | SCHEMBL190737 | 3-(3-trimethoxysilylpropyl)oxolane-2, 5-dione | trimethoxysilylpropyl succinic anhydride | 3-trimethox

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

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

≥95%

Nombres e identificadores

• Sonrisas canónicas: CO[Si](CCCC1CC(=O)OC1=O)(OC)OC
• IUPAC Name: 3-(3-trimethoxysilylpropyl)oxolane-2,5-dione
• InChIKey: ZADOWCXTUZWAKL-UHFFFAOYSA-N
• INCHI: 1S/C10H18O6Si/c1-13-17(14-2,15-3)6-4-5-8-7-9(11)16-10(8)12/h8H,4-7H2,1-3H3
• Isómeros SMILES: CO[Si](CCCC1CC(=O)OC1=O)(OC)OC
• PubChem CID: 11507216
• Peso molecular: 262.33

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Clase Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Alkoxysilanes
          • Level6 Trialkoxysilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Clase: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Alkoxysilanes
• Direct Parent: Trialkoxysilanes
• Alternative Parents: Dicarboxylic acids and derivatives Oxolanes Carboxylic acid anhydrides Silyl ethers Lactones Oxacyclic compounds Organoheterosilanes Organic metalloid salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Trialkoxysilane - Dicarboxylic acid or derivatives - Carboxylic acid anhydride - Oxolane - Lactone - Silyl ether - Organoheterocyclic compound - Organoheterosilane - Carboxylic acid derivative - Organic metalloid salt - Oxacycle - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organooxygen compound - Organic oxygen compound - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as trialkoxysilanes. These are organosilicon compounds with the general formula RO[Si](R')(OR'')OR''' (R-R''' = aliphatic organyl group).
• 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: Moisture &Heat sensitive
• Índice de refracción: 1.45
• Punto de inflamación (°C): 190 °C
• Peso molecular: 262.330 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 7
• Exact Mass: 262.087 Da
• Monoisotopic Mass: 262.087 Da
• Topological Polar Surface Area: 71.100 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 280.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

XLogP3

Referencias

1. Fuad Abduro Bushira, Shimeles Addisu Kitte, Yong Wang, Haijuan Li, Ping Wang, Yongdong Jin.  (2021)  Plasmon-Boosted Cu-Doped TiO2 Oxygen Vacancy-Rich Luminol Electrochemiluminescence for Highly Sensitive Detection of Alkaline Phosphatase.  ANALYTICAL CHEMISTRY,      [PMID:34743510] [10.1021/acs.analchem.1c03842]

2. Wenyue Zhang, Ziyi Li, Xiaoli Lun, Yingshu Guo.  (2024)  Telomerase-Responsive CRISPR System-Regulated Nanobomb for Triggering Research on Telomerase “Self-Detonation”.  ACS Applied Materials & Interfaces,      [PMID:39679901] [10.1021/acsami.4c18859]