1116-61-6

Usage

Uses

Used in Pharmaceutical Industry:
Tri-N-Propylboron is used as a catalyst and reagent for the synthesis of various pharmaceutical compounds. Its ability to facilitate hydroboration and Suzuki coupling reactions makes it a valuable component in the development of new and innovative drugs.
Used in Agrochemical Industry:
In the agrochemical industry, Tri-N-Propylboron serves as a catalyst and reagent in the production of agrochemicals. Its role in organic synthesis aids in the creation of effective and targeted agrochemical products.
Used in Polymer Industry:
Tri-N-Propylboron is utilized as a catalyst and reagent in the synthesis of polymers. Its contribution to organic synthesis enables the development of polymers with specific properties and applications.
Used in Organic Synthesis:
Tri-N-Propylboron is used as a versatile catalyst and reagent in organic synthesis. Its ability to undergo hydroboration and Suzuki coupling reactions makes it an essential component in the synthesis of a wide range of organic compounds.

InChI:InChI=1/C9H21B/c1-4-7-10(8-5-2)9-6-3/h4-9H2,1-3H3

Upstream product

• 60-29-7 diethyl ether 
• 1095-03-0 triphenylborane 
• 927-77-5 n-propylmagnesium bromide 
• 96080-52-3 dipropyl phenylboronate 
• 102-24-9 cyclotriboric acid trimethyl ester 
• 628-91-1 di-n-propyl zinc 
• 10557-57-0 propylmagnesium iodide 
• 2234-82-4 1-propylmagnesium chloride 
• 187737-37-7 propene 
• 19287-45-7 diborane 
• 7637-07-2 boron trifluoride 
• 77333-20-1 3,5-bis(dimethylamino)-1,2,4,3,5-trithiaborolane 
• 22784-01-6 tetrapropyldiborane⁽⁶⁾ 
• 109-97-7 pyrrole 

Downstream Products

• 17745-45-8 propylboronic acid 
• 4443-46-3 Dipropylthioborsaeure-phenylester 
• 4540-98-1 (n-C3H7)2BNHC6H5 
• 14108-08-8 3-phenyl-1-propyl-2,3-dihydro-1H-benzo[b]borole 
• 14108-07-7 2-phenyl-1-propyl-2,3-dihydro-1H-benzo[b]borole 
• 3844-94-8 1-(trimethylsilyl)-1-hexyne 
• 27829-72-7 ethyl (E)-hex-2-enoate 
• 3521-91-3 hept-1-en-4-ol 
• 30312-51-7 1-benzyl-2-propyl-1.2-azaborolane 
• 56305-38-5 3-Octenyl-phenyl-keton 
• 57984-32-4 4,5-dipropyl-4-octene 
• 67562-22-5 4,4,6-trimethyl-2-propyl-[1,3,2]dioxaborinane 
• 67562-19-0 4,4,5,5-tetramethyl-2-n-propyl-1,3,2-dioxaborolane 
• 16205-90-6 ethyl 2-hexynoate 

Relevant academic research and scientific papers

METHOD FOR PRODUCING TRIHYDROCARBYLBORANE

The present invention provides a method for industrial production of trihydrocarbylborane which method is excellent both in quality and in cost. The present invention is concerned with production of trihydrocarbylborane, comprising a reaction synthesizing the trihydrocarbylborane and aluminum oxide from trihydrocarbylboroxine and trihydrocarbylaluminum, characterized in that the reaction is allowed to proceed so that the trihydrocarbylaluminum is present at the end of the reaction in an amount of 0.5 moles or more per mole of the aluminum oxide produced in the reaction.

Reactions of Diphenylphosphane Oxide with Organodiboranes(6) - Structure of a Zwitterionic Compound

(C6H5)2POB(C2H5)2 (3'a), prepared from diphenylphosphane oxide (C6H5)2P(O)H (1) and activated triethylborane (2a*), reacts with tetraalkyldiboranes(6) (R2BH)2 to form the BH3-addition compounds (C6H5)2P(BH3)OBR2 , 2BR , and 3B .The reaction of bis(9-borabicyclononane) (4c)2 with 1 leads to (C6H5)2POBC8H14 (3'c) or 3'c-4a and (C6H5)2PH (7) or (C6H5)2PH-HBC8H14 (7-4c).The crystalline zwitterionic (C6H5)2P(H)OB3 (X-ray analysis) is isolated from the reaction of 1 with (4a)2.