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

CAS: 10416-59-8 Cat. No.: T131644 Formula: C₈H₂₁NOSi₂ Peso molecolare: 203.43 Beilstein Registry Number: 1306669 Numero EC: 233-892-7

QUALITÀ & PUREZZA 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

Specifiche

Sinonimi

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

Specifiche e purezza

for GC derivatization

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

for GC derivatization

Nomi e identificatori

Pubchem Sid

508810796

Sorrisi canonici

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

Isomeri SMILES

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

WGK Germania

3

RTECS

AK3000000

Peso molecolare

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
• Descrizione: 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

Proprietà chimiche e fisiche

• Sensibilità: Moisture Sensitive
• Indice di rifrazione: 1.417
• Punto di infiammabilità (°F): 107.6℉
• Punto di infiammabilità (°C): 42°C
• Punto di ebollizione (°C): 71-73°C
• Punto di fusione (°C): 24°C
• Peso molecolare: 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

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