796857-59-5 Usage
Uses
Used in Chemical Industry:
Benzenemethanamine,N,N',N''-(2,4,6-boroxintriyltri-4,1-phenylene)tris[N-(phenylmethyl)(9CI) is used as a catalyst for various organic reactions, such as polymerization and cross-coupling reactions, due to its high thermal stability and reactivity.
Used in Pharmaceutical Chemistry:
Benzenemethanamine,N,N',N''-(2,4,6-boroxintriyltri-4,1-phenylene)tris[N-(phenylmethyl)(9CI) is used as a reagent in the production of various pharmaceuticals and fine chemicals, contributing to the development of new drugs and therapeutic agents.
Used in Polymer Materials:
Benzenemethanamine,N,N',N''-(2,4,6-boroxintriyltri-4,1-phenylene)tris[N-(phenylmethyl)(9CI) has potential applications as a flame retardant and photoinitiator in polymer materials, enhancing their performance and safety.
Used in Organic Synthesis:
It is utilized as a versatile catalyst in organic synthesis, enabling the synthesis of complex organic compounds and facilitating various chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 796857-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,6,8,5 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 796857-59:
(8*7)+(7*9)+(6*6)+(5*8)+(4*5)+(3*7)+(2*5)+(1*9)=255
255 % 10 = 5
So 796857-59-5 is a valid CAS Registry Number.
796857-59-5Relevant academic research and scientific papers
Process for the preparation of aniline boronic acids and derivatives thereof
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Page 8, (2010/02/09)
Production of anilineboronic acid derivatives (I) comprises converting an aniline compound (II) to a doubly protected derivative (III), metallating (III) and simultaneously or subsequently reacting it with a borate ester (IV) to give a protected anilineboronic acid ester (V), and deprotecting (V). Production of anilineboronic acid derivatives of formula (I) comprises converting an aniline compound of formula (II) to a doubly protected derivative of formula (III), metallating (III) and simultaneously or subsequently reacting it with a borate ester of formula (IV) to give a protected anilineboronic acid ester of formula (V), and deprotecting (V): [Image] PG : protecting group; R : H, halo, 1-20C alkyl or alkoxy, optionally substituted 6-12C aryl or aryloxy, heteroaryl or heteroaryloxy, optionally substituted 3-8C cycloalkyl, dialkylamino, diarylamino, alkylthio, arylthio, ester or acetal; X : H or halo; R1>-R3>H or optionally substituted 1-20C alkyl, or two of R1>-R3> can form a ring or another borate group.
