N-(Trimethylsilyl)acetamide

N-(Trimethylsilyl)acetamide
  • CAS No.:13435-12-6
Other grades of this product :

N-(Trimethylsilyl)acetamide Basic information
Product Name:N-(Trimethylsilyl)acetamide
Synonyms:N-(TRIMETHYLSILYL)ACETAMIDE FOR SYNTHESI;N-(Trimethylsilyl)acetamide,97%;N-(Trimethylsilyl);(acetylamino)trimethylsilane;n-(trimethylsilyl)-acetamid;N-TRIMETHYLSILYLACETAMIDE;TRIMETHYLSILYLACETAMIDE;TMSA
CAS:13435-12-6
MF:C5H13NOSi
MW:131.25
EINECS:236-565-7
Product Categories:Aliphatics;Miscellaneous Reagents;Analytical Chemistry;GC Derivatizing Reagents;Si (Classes of Silicon Compounds);Silicon Compounds (for Synthesis);Silylacetamides;Silylation (GC Derivatizing Reagents);Si-N Compounds;Synthetic Organic Chemistry;Trimethylsilylation (GC Derivatizing Reagents)
Mol File:13435-12-6.mol
N-(Trimethylsilyl)acetamide Chemical Properties
Melting point 46-49 °C(lit.)
Boiling point 84 °C18 mm Hg(lit.)
density 0.859±0.06 g/cm3(Predicted)
Fp 135 °F
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform, DMSO, Methanol
form Crystalline Mass
pka18.23±0.46(Predicted)
color White to yellow
Water Solubility reacts
Hydrolytic Sensitivity7: reacts slowly with moisture/water
Sensitive Moisture Sensitive
BRN 741928
Stability:Moisture Sensitive
CAS DataBase Reference13435-12-6(CAS DataBase Reference)
EPA Substance Registry SystemAcetamide, N-(trimethylsilyl)- (13435-12-6)
Safety Information
Hazard Codes Xi-F,Xi,F
Risk Statements 36/37/38-11
Safety Statements 37/39-26
RIDADR 1325
WGK Germany 3
RTECS AD0250000
10-21
TSCA Yes
HazardClass 4.1
PackingGroup III
HS Code 29319090
MSDS Information
ProviderLanguage
SigmaAldrichEnglish
ACROSEnglish
ALFAEnglish
N-(Trimethylsilyl)acetamide Usage And Synthesis
Chemical PropertiesWHITE TO YELLOWISH CRYSTALLINE MASS
UsesN-Trimethylsilylacetamide is a silylating agent used in organic synthesis. N-Trimethylsilylacetamide is used in the preparation of the antibacterial agent Cefdinir (C242670).
General DescriptionThe efficiency of N-(Trimethylsilyl)acetamide (TMS acetamide) as allyl group scavenger and its compatibility with Fluorenylmethyloxycarbonyl chloride (Fmoc) protecting groups were studied.
Purification MethodsDistil the amide repeatedly in an inert atmosphere with all operations to be performed in an anhydrous atmosphere. In the presence of moisture, trimethylsilanol (b 31-34o/26mm) is formed and is a likely impurity (check by NMR). [Birkofer et al. Chem Ber 96 1473 1963, Beilstein 4 IV 4011.]
N-(Trimethylsilyl)acetamide Preparation Products And Raw materials
Preparation ProductsCefdinir-->2-METHYL-1-(TRIMETHYLSILOXY)-1-PROPENE-->1-(Trimethylsiloxy)cyclopentene

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