CAS#:20160-71-8 N-Trimethylsilylmethyl-N'.N'-diphenyl-harnstoff
![CAS#:20160-71-8 N-Trimethylsilylmethyl-N'.N'-diphenyl-harnstoff](https://www.chemsrc.com/caspic/289/20160-71-8.png)
N,O-Bis(trimethylsilyl)trifluoroacetamide with trimethylchlorosilane (CAS 25561-30-2)
![](https://media.scbt.com/product/n-o-bis-trimethylsilyl-trifluoroacetamide-with-trimethylchlorosilane-25561-30-2-_20_42_b_204282.jpg)
N,O-Bis(trimethylsilyl)trifluoroacetamide with trimethylchlorosilane | CAS 25561-30-2
![](https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/structures/220/396/7bbb542e-c987-4db8-a96a-e2b54ab99c5f/640/7bbb542e-c987-4db8-a96a-e2b54ab99c5f.png)
Trimethylsilyl)methacrylate 98 13688-56-7
![](https://www.chemsrc.com/caspic/289/20160-71-8.png)
CAS#:20160-71-8, N-Trimethylsilylmethyl-N'.N'-diphenyl-harnstoff
Trimethylsilanol sodium salt. Sodium trimethylsilanolate is used as a catalyst in the: Synthesis of the rhodium silonate complex. Silylation of methylphenylsilane with tert-butyldimethylsilanol to synthesize trisiloxanes. Sodium trimethylsilanolate is a versatile and very powerful reagent for the conversion of esters to carboxylic acids and the hydrolysis of nitriles to primary amides.
![](https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/structures/913/013/012e060a-5c03-45d8-ad79-c16649e329bd/640/012e060a-5c03-45d8-ad79-c16649e329bd.png)
Sodium trimethylsilanolate, CAS 18027-10-6, 95%
![](https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/structures/816/258/07445a7c-fdef-4f54-9b73-354f1cc9e738/640/07445a7c-fdef-4f54-9b73-354f1cc9e738.png)
1,3-Diphenylurea 98 102-07-8
![](https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/structures/217/997/61dd2f40-6406-4f3d-a32b-3c40dc5d08f7/640/61dd2f40-6406-4f3d-a32b-3c40dc5d08f7.png)
N,N-Dimethyltrimethylsilylamine 97 2083-91-2
![](https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/structures/304/002/0761a989-ef7d-4ff1-83a4-a4acbe8cb457/640/0761a989-ef7d-4ff1-83a4-a4acbe8cb457.png)
1,1,3,3-Tetramethyl-1,3-diphenyldisilazane 96 3449-26-1
Forms azomethine ylides which readily undergo [3+2] cycloaddition to α,ß-unsaturated esters affording N-benzyl substituted pyrrolidines in good yields.
![](https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/structures/217/410/c76a8a57-986a-4be6-9a92-8999596ec016/640/c76a8a57-986a-4be6-9a92-8999596ec016.png)
N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine, CAS 93102-05-7, 96%
![](https://www.biosynth.com/storage/ChemAxonStructureImages/HX/C7/HXC77635_structure.png)
FD162318, 943757-71-9