TMS-BA - for GC derivatization , CAS No.10416-59-8

CAS: 10416-59-8 Cat. No.: T131644 Fórmula: C₈H₂₁NOSi₂ Peso molecular: 203.43 Beilstein Registry Number: 1306669 Número CE: 233-892-7

GRAU & PUREZA for GC derivatization

Synonyms

B0510 | DTXSID5051525 | D72517 | Trimethylsilyl N-(trimethylsilyl)ethanimidoate | TMS-BA | N-trimethylsilyl-acetylimidic acid trimethylsilyl ester | trimethylsilyl N-trimethylsilylacetimidate | BCP24460 | n,o-bis (trimethylsilyl)acetamide | (E)-trimethyls

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Especificações

Sinónimos

B0510 | DTXSID5051525 | D72517 | Trimethylsilyl N-(trimethylsilyl)ethanimidoate | TMS-BA | N-trimethylsilyl-acetylimidic acid trimethylsilyl ester | trimethylsilyl N-trimethylsilylacetimidate | BCP24460 | n,o-bis (trimethylsilyl)acetamide | (E)-trimethyls

Especificações e pureza

for GC derivatization

Condições de armazenamento de armazenamento

Store at 2-8°C,Argon charged

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Grau

for GC derivatization

Nomes e identificadores

Pubchem Sid

508810796

Sorrisos canónicos

CC(=N[Si](C)(C)C)O[Si](C)(C)C

IUPAC Name

trimethylsilyl N-trimethylsilylethanimidate

InChIKey

SIOVKLKJSOKLIF-UHFFFAOYSA-N

INCHI

1S/C8H21NOSi2/c1-8(9-11(2,3)4)10-12(5,6)7/h1-7H3

SMILES isoméricas

CC(=N[Si](C)(C)C)O[Si](C)(C)C

WGK Alemanha

3

RTECS

AK3000000

Peso molecular

203.43

Beilstein

1306669

Reaxy-Rn

1306669

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Classe Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Organoheterosilanes
          • Level6 Trialkylheterosilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Classe: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Organoheterosilanes
• Direct Parent: Trialkylheterosilanes
• Alternative Parents: Organic metalloid salts N-silyl compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkylheterosilane - N-silyl compound - Organic metalloid salt - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organonitrogen compound - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as trialkylheterosilanes. These are organoheterosilanes, bearing a silicon atom linked to three alkyl groups and one 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

Propriedades químicas e físicas

• Sensibilidade: Moisture Sensitive
• Índice de refração: 1.417
• Ponto de inflamação (°F): 107.6℉
• Ponto de inflamação (°C): 42°C
• Ponto de ebulição (°C): 71-73°C
• Ponto de fusão (°C): 24°C
• Peso molecular: 203.430 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 203.116 Da
• Monoisotopic Mass: 203.116 Da
• Topological Polar Surface Area: 21.600 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 176.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 1
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1

XLogP3