91059-43-7 Usage
Chemical structure
Naphthalene core with iodine at position 1 and carboxylic acid at position 2.
Derivative of naphthalene
Modified version of the parent compound naphthalene.
Carboxylic acid functional group
Presence of -COOH group in the molecule.
Iodine substituent
An iodine atom attached to the naphthalene ring at position 1.
Building block in organic synthesis
Used as a starting material for creating other organic compounds.
Potential use in chemical reactions
Possesses reactivity that allows it to participate in various chemical processes.
Precursor for synthesis of other organic compounds
Acts as an intermediate in the production of other molecules.
Valuable tool for material and pharmaceutical development
Contributes to the creation of new substances in material science and drug discovery.
Reagent in research laboratories
Utilized in different chemical reactions for experimental purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 91059-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,5 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91059-43:
(7*9)+(6*1)+(5*0)+(4*5)+(3*9)+(2*4)+(1*3)=127
127 % 10 = 7
So 91059-43-7 is a valid CAS Registry Number.
91059-43-7Relevant articles and documents
Catalytic enantioselective α-tosyloxylation of ketones using iodoaryloxazoline catalysts: Insights on the stereoinduction process
Guilbault, Audrey-Anne,Basdevant, Benoit,Wanie, Vincent,Legault, Claude Y.
, p. 11283 - 11295 (2013/02/23)
A family of iodooxazoline catalysts was developed to promote the iodine(III)-mediated α-tosyloxylation of ketone derivatives. The α-tosyloxy ketones produced are polyvalent chiral synthons. Through this study, we have unearthed a unique mode of stereoinduction from the chiral oxazoline moiety, where the stereogenic center alpha to the oxazoline oxygen atom is significant. Computational chemistry was used to rationalize the stereoinduction process. The catalysts presented promote currently among the best levels of activity and selectivity for this transformation. Evaluation of the scope of the reaction is presented.
Iodosonaphthoate catalysts for the cleavage of a reactive phosphate
Moss, Robert A.,Zhang, Hongmei,Chatterjee, Swati,Krogh-Jespersen, Karsten
, p. 1729 - 1732 (2007/10/02)
Iodosonaphthoates 3-5 are potent catalysts for the hydrolysis of P-nitro-phenyldiphenyl phosphate.
