Triisopropylsilane(TIPS) - ≥98% , CAS No.6485-79-6

CAS: 6485-79-6 Cat. No.: T107280 Fórmula: C₉H₂₂Si Peso molecular: 158.36 Beilstein Registry Number: 1733718 Número EC: 464-880-1

GRADE & PURITY ≥98%

Synonyms

EN300-117959 | J-525100 | tris(propan-2-yl)silane | PD118098 | AKOS006222744 | AS-19155 | Aksci Bulk ReagentTriisopropylsilane | Triisopropylsilane, 98% | A14931 | AKOS030228028 | Benzenesulfonic acid,5-[(4-amino-1-naphthalenyl)azo]-2-[2-[4-[(2-hydroxy-1-

Storage

Room temperature,Argon charged

Shipped In

Normal

Descripción general

Triisopropylsilane (TIPS) is an organosilicon compound that is low in toxicity, easy to handle, and capable of selectively reducing various functional groups, making it suitable as a reducing agent in organic synthesis. In the presence of Lewis acids (e.g., titanium tetrachloride), it can selectively reduce ketones and aldehydes to their corresponding alkanes, and epoxides to their corresponding alcohols.

Specifications

Sinónimos

EN300-117959 | J-525100 | tris(propan-2-yl)silane | PD118098 | AKOS006222744 | AS-19155 | Aksci Bulk ReagentTriisopropylsilane | Triisopropylsilane, 98% | A14931 | AKOS030228028 | Benzenesulfonic acid,5-[(4-amino-1-naphthalenyl)azo]-2-[2-[4-[(2-hydroxy-1-

Especificaciones y pureza

≥98%

Aplicación

Triisopropylsilane can be used as a reducing agent: In the synthesis of 4-pyrrolobenzoyl peptides during solid-phase peptide synthesis. In the reaction of amides with hydrosilanes catalyzed by transition metal complexes. For the selective reduction of C-a

Condiciones de almacenamiento de almacenamiento

Room temperature,Argon charged

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

Pubchem Sid

504764056

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504764056

Sonrisas canónicas

CC(C)[Si](C(C)C)C(C)C

InChIKey

ZGYICYBLPGRURT-UHFFFAOYSA-N

INCHI

1S/C9H21Si/c1-7(2)10(8(3)4)9(5)6/h7-9H,1-6H3

Isómeros SMILES

CC(C)[Si](C(C)C)C(C)C

WGK Alemania

3

Número ONU

1993

Peso molecular

158.36

Beilstein

1733718

Reaxy-Rn

1733718

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Hydrocarbon derivatives

• Kingdom: Organic compounds
• Superclass: Hydrocarbon derivatives
• Clase: Not available
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Hydrocarbon derivatives
• Alternative Parents: Organosilicon compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Organosilicon compound - Organic metalloid moeity - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as hydrocarbon derivatives. These are derivatives of hydrocarbons obtained by substituting one or more carbon atoms by an heteroatom. They contain at least one carbon atom and heteroatom.
• 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: Immiscible with water.
• Sensibilidad: Moisture sensitive.
• Índice de refracción: 1.434
• Punto de inflamación (°F): 100.4 °F
• Punto de inflamación (°C): 38 °C
• Punto de ebullición (°C): 84-86 °C/35 mmHg (lit.)
• Peso molecular: 157.350 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 157.141 Da
• Monoisotopic Mass: 157.141 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 65.700
• 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

XLogP3