351422-73-6 Usage
Chemical Properties
White to brown solid
Uses
Different sources of media describe the Uses of 351422-73-6 differently. You can refer to the following data:
1. Reactant involved in the synthesis of a variety of inhibitors including:Orally active phosphodiesterase 10A inhibitorsPyrimidine derivatives as TpI2 kinase inhibitorsPeptidomimetic inhibitors of STAT3 proteinReactant involved in:Oxidative cross-coupling with mercaptoacetylenesTrifluoromethylation via a Collidine trifluoromethylating agentSuzuki cross-coupling reactions
2. Reactant involved in the synthesis of a variety of inhibitors including:? ;Orally active phosphodiesterase 10A inhibitors1? ;Pyrimidine derivatives as TpI2 kinase inhibitors2? ;Peptidomimetic inhibitors of STAT3 protein3Reactant involved in:? ;Oxidative cross-coupling with mercaptoacetylenes4? ;Trifluoromethylation via a Collidine trifluoromethylating agent5? ;Suzuki cross-coupling reactions6
3. suzuki reaction
Check Digit Verification of cas no
The CAS Registry Mumber 351422-73-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,4,2 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 351422-73:
(8*3)+(7*5)+(6*1)+(5*4)+(4*2)+(3*2)+(2*7)+(1*3)=116
116 % 10 = 6
So 351422-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H8BNO3/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4,11-12H,(H2,9,10)
351422-73-6Relevant articles and documents
METHOD FOR THE PRODUCTION OF BORONIC ACIDS CARRYING CYANOALKYL, CARBOXYL AND AMINOCARBONYL GROUPS AND THEIR DERIVATIVES
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Page/Page column 5, (2009/12/05)
A process for the manufacture of aminocarbonyl boronic acids of formula (IV) by converting the compounds of formula (III) with a Br?nsted base Y(OH)n in a solvent or a solvent mixture, in which Z represents an optionally substituted arylene, heteroarylene, alkene, heteroalkene, alkylidene, heteroalkylidene, alkenylidene, heteroalkenylidene, alkynylidene, arylalkylene, heteroarylalkylene, arylheteroalkylene, heteroarylheteroalkylene, alkylheteroarylene, heteroalkylheteroarylene, or alkylarylene group; Y represents a metal or ammonium cation of valence n with 0n5; and B represents boronic acid, boronic acid ester, or a borate, or a boronic acid anhydride. The aminocarbonyl boronic acids of formula (IV) can be further hydrolyzed to form the carboxy boronic acid of formula (V).
