388606-32-4 Usage
Uses
Used in Organic Synthesis:
3-[(2,2-DIMETHYL-1,2-AZASILOLIDIN-1-YL)-(DIMETHYL)-SILYL]-1-PROPANAMINE is used as a reagent in organic synthesis for its ability to facilitate specific chemical reactions, contributing to the formation of desired products with high selectivity and efficiency.
Used in Asymmetric Catalysis:
In the field of asymmetric catalysis, 3-[(2,2-DIMETHYL-1,2-AZASILOLIDIN-1-YL)-(DIMETHYL)-SILYL]-1-PROPANAMINE is utilized as a catalyst to promote enantioselective reactions, enabling the production of chiral molecules with a specific three-dimensional arrangement, which is crucial in pharmaceutical development and other chemical industries.
Used in Pharmaceutical Compound Preparation:
3-[(2,2-DIMETHYL-1,2-AZASILOLIDIN-1-YL)-(DIMETHYL)-SILYL]-1-PROPANAMINE is used as a building block in the preparation of pharmaceutical compounds, where its unique structural features can contribute to the development of new drugs with improved properties, such as enhanced bioavailability and targeted therapeutic effects.
Used as a Ligand in Transition-Metal Catalyzed Reactions:
In transition-metal catalyzed reactions, 3-[(2,2-DIMETHYL-1,2-AZASILOLIDIN-1-YL)-(DIMETHYL)-SILYL]-1-PROPANAMINE serves as a ligand, enhancing the catalytic activity and selectivity of the metal center. This application is particularly important in the synthesis of complex organic molecules and the development of new catalytic processes in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 388606-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,8,6,0 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 388606-32:
(8*3)+(7*8)+(6*8)+(5*6)+(4*0)+(3*6)+(2*3)+(1*2)=184
184 % 10 = 4
So 388606-32-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H26N2Si2/c1-13(2,9-5-7-11)12-8-6-10-14(12,3)4/h5-11H2,1-4H3
388606-32-4Relevant articles and documents
METHOD FOR PRODUCING AMINO-ORGANOSILANES
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Page/Page column 6, (2011/07/29)
In the preparation of aminoorganylsilanes and cyclic aminosilanes by reaction of an organyl amine with a haloorganylsilane, the byproduct halide salt of the amine reactant is decomposed to amine by addition of a base whose halide salt forms a liquid phase at a temperature below 200° C., and the liquid base halide is separated from the reaction mixture.
Cyclic silazanes
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, (2008/06/13)
The invention relates to cyclic silazanes of the formula II in which R is a divalent, Si—C and C—N-bound, optionally cyano- or halogen-substituted C3-C15-hydrocarbon radical, in which one or more, non-adjacent methylene units may be replaced by —O—, —CO—, —COO—, —OCO—, —OCOO—, —S— or —NRX— groups and in which one or more non-adjacent methine units may be replaced by —N═, —N═N— or —P═ groups, where at least 3 and at most 6 atoms are arranged between the silicon atom and the nitrogen atom of the ring, RXis hydrogen or an optionally halogen-substituted C1-C10-hydrocarbon radical, and R2is a hydrogen atom or a monovalent, optionally cyano- or halogen-substituted, Si-C- bound C1-C20-hydrocarbon radical or C1-C20-hydrocarbonoxy radical, in each of which one or more non-adjacent methylene units may be replaced by —O—, —CO—, —COO—, —OCO—, —OCOO—, —S— or —NRX— groups and in which one or more non-adjacent methine units may be replaced by —N═, —N═N— or —P═ groups.
