38850-27-0

Basic information

• Product Name: Benzamide, N,N-bis(trimethylsilyl)-
• CAS NO: 38850-27-0
• Molecular Formula: C13H23NOSi2
• Molecular Weight: 265.503
• Mol File: 38850-27-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzamide, N,N-bis(trimethylsilyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N,N-bis(trimethylsilyl)-(38850-27-0)
• EPA Substance Registry System: Benzamide, N,N-bis(trimethylsilyl)-(38850-27-0)

Safety Data

• Hazardous Substances Data: 38850-27-0(Hazardous Substances Data)

Upstream product

• 75-79-6 Methyltrichlorosilane 
• 22180-78-5 N,N-dichloro-benzamide 
• 455-32-3 benzoyl fluoride 
• 65-85-0 benzoic acid 
• 1070-89-9 sodium hexamethyldisilazane 
• 618-38-2 benzoyl iodide 
• 1357556-77-4 N-triethylgermyl-N,N-bis(trimethylsilyl)amine 
• 268208-86-2 N-triethylstannyl-N,N-bis(trimethylsilyl)amine 
• 1586-73-8 tris(trimethylsilyl)amine 

Downstream Products

• 25922-45-6 Triphenylarsin N-benzoylimin 
• 87786-72-9 2,6-diphenyl-4-phenylsulfonylimino-5,6-dihydro-4,1,3-selenaoxazine 
• 87786-79-6 4-Chloro-N-[2,6-diphenyl-5,6-dihydro-4λ⁴-[1,4,3]oxaselenazin-(4Z)-ylidene]-benzenesulfonamide 
• 70890-23-2 2,6-diphenyl-4,4-dichloro-5,6-dihydro-4,1,3-selenaoxazine 
• 95477-24-0 (2-phenyl-2-benzoyloxyethyl)methoxyselenium dichloride 
• 70890-24-3 C₇H₅Cl₂NOSe 
• 61945-93-5 N,N'-dibenzoylselenium diimide 
• 87786-82-1 N-p-chlorophenylsulfonyl-N'-benzoylselenium diimide 
• 61706-76-1 2-trimethylsiloxy-4,5-benzo-1,3,2-dioxaphospholane 
• 100-47-0 benzonitrile 
• 20043-21-4 N-Benzoylthionylimide 
• 71877-44-6 C₁₄H₁₂N₂O₃SSe 
• 71877-41-3 N-phenylsulfonyl-N'-benzoylselenium diimide 

Relevant articles and documents

Direct amidation of acid fluorides using germanium amides

Amide functional groups are an essential linkage that are found in peptides, proteins, and pharmaceuticals and new methods are constantly being sought for their formation. Here, a new method for their preparation is presented where germanium amides Ph3GeNR2convert acid fluorides directly to amides. These germanium amides serve to abstract the fluorine atom of the acid fluoride and transfer their amide group -NR2to the carbonyl carbon, and so function as amidation reagents.

TRIMETHYLSILYLATION OF COMPOUNDS WITH AN N-Cl BOND

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