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N,N-Bis(trimethylsilyl)formamide

CAS No.
15500-60-4
Chemical Name:
N,N-Bis(trimethylsilyl)formamide
Synonyms
BSF;N,N-BIS(TRIMETHYLSILYL)FORMAMIDE;n,n-bis(trimethylsilyl)-formamid;BIS-N N-(TRIMETHYLSILYL)FORMAMIDE;Formamide, N,N-bis(trimethylsilyl)-;BIS-N N-(TRIMETHYLSILYL)FORMAMIDE 97%;N,N-Bis-(trimethylsilyl)-formamide(BSF)
CBNumber:
CB8480743
Molecular Formula:
C7H19NOSi2
Molecular Weight:
189.4
MDL Number:
MFCD00014849
MOL File:
15500-60-4.mol
MSDS File:
SDS
Last updated:2023-05-04 15:13:22

N,N-Bis(trimethylsilyl)formamide Properties

Melting point 158 °C
Boiling point 158 °C
Density 0.885 g/mL at 20 °C(lit.)
refractive index n20/D 1.437
Flash point 37 °C
solubility benzene, CCl4, CH2Cl2, CHCl3.
pka 0.16±0.70(Predicted)
CAS DataBase Reference 15500-60-4(CAS DataBase Reference)
FDA UNII FXX3KFS75F
EPA Substance Registry System Formamide, N,N-bis(trimethylsilyl)- (15500-60-4)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS02
Signal word  Warning
Hazard statements  H226
Risk Statements  10
RIDADR  UN 1993 3/PG 3
WGK Germany  3
10-21
HazardClass  3.2
PackingGroup  III

N,N-Bis(trimethylsilyl)formamide price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation ING0004531 N,N-BIS(TRIMETHYLSILYL)FORMAMIDE 95.00% 15500-60-4 5G $132.3 2021-12-16 Buy
AHH MT-55585 N,N-Bis(trimethylsilyl)formamide 90% 15500-60-4 50ml $230 2021-12-16 Buy
Product number Packaging Price Buy
ING0004531 5G $132.3 Buy
MT-55585 50ml $230 Buy

N,N-Bis(trimethylsilyl)formamide Chemical Properties,Uses,Production

Physical properties

81–82 °C/20 mmHg; 154 °C/760 mmHg; mp 16–17 °C; n20 D 1.4388.

Uses

N,N-Bis(trimethylsilyl)formamide can be used as source of nucleophilic formamide and N-silylaldimine synthon.
N,N-Bis(trimethylsilyl)formamide (BSF) exists in the amide form with both silyl groups attached to the nitrogen atom. This is in contrast to most other bis(TMS)amides (e.g., bis(TMS)- acetamide), which favor the N,O-bis(TMS)imidate isomer. BSF behaves as an N-formamido nucleophile, reacting with the carbonyl group of aldehydes and activated ketones to give N-formyl-O-trimethylsilyl-N,O-acetals. Similarly, reaction with imines (or their precursors) can in some cases give N-formylN,N-acetals. BSF undergoes reactions with a range of other electrophiles including acid chlorides, chloroformate esters, and isocyanates to give a range of interesting products. When treated with organolithium nucleophiles, attack occurs at the carbonyl function, to provide N-silylaldimines after elimination of a silyloxy unit. Such imines are reported to undergo further reactions to give heterocycles. There are also reports of BSF acting as a silylating agent, to give silyl enol ethers, although it is not commonly used for this application.

Preparation

chlorotrimethylsilane was added at room temperature to a solution of formamide and triethylamine in dry benzene and the mixture was heated at reflux for 1 h. The reaction mixture was filtered, and the filtrate was evaporated to give a crude oil. This was purified by high-vacuum distillation to afford N,N-bis(trimethylsilyl)formamide (BSF) as an oil in 75% yield.

15500-60-4 synthesis

N,N-Bis(trimethylsilyl)formamide Preparation Products And Raw materials

Raw materials

Preparation Products

N,N-Bis(trimethylsilyl)formamide Suppliers

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CR Corporation Lomited
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n,n-bis(trimethylsilyl)-formamid N,N-BIS(TRIMETHYLSILYL)FORMAMIDE BSF BIS-N N-(TRIMETHYLSILYL)FORMAMIDE N,N-Bis-(trimethylsilyl)-formamide(BSF) BIS-N N-(TRIMETHYLSILYL)FORMAMIDE 97% Formamide, N,N-bis(trimethylsilyl)- 15500-60-4 C7H19NOSi2 Analytical Chromatography Product Catalog Fluka Reagents Derivatization Reagents