153074-91-0 Usage
Description
4-(BOC-AMIDINO)-BENZOIC ACID is a benzoic acid derivative that serves as a building block in organic synthesis for creating pharmaceuticals and other organic compounds. The BOC group acts as a protecting group for the amidino functionality in the molecule.
Uses
Used in Pharmaceutical Industry:
4-(BOC-AMIDINO)-BENZOIC ACID is used as a key intermediate in the synthesis of peptide-based drugs, contributing to the development of new medications.
Used in Organic Chemistry:
4-(BOC-AMIDINO)-BENZOIC ACID is used as a reagent in various organic chemistry reactions, facilitating the formation of complex organic molecules.
Used in Medicinal Chemistry Research:
4-(BOC-AMIDINO)-BENZOIC ACID is utilized in medicinal chemistry for the design and synthesis of potential therapeutic agents, enhancing drug discovery efforts.
Used in Biochemistry:
4-(BOC-AMIDINO)-BENZOIC ACID is employed in biochemistry to study the interactions of various biomolecules, aiding in the understanding of biological processes and the development of targeted therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 153074-91-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,0,7 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 153074-91:
(8*1)+(7*5)+(6*3)+(5*0)+(4*7)+(3*4)+(2*9)+(1*1)=120
120 % 10 = 0
So 153074-91-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N2O4/c1-13(2,3)19-12(18)15-10(14)8-4-6-9(7-5-8)11(16)17/h4-7H,1-3H3,(H,16,17)(H2,14,15,18)
153074-91-0Relevant articles and documents
Acetic acid derivatives
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, (2008/06/13)
Acetic acid derivatives of the formula STR1 wherein L, M, T and Q have the significance given in the description, can be used for the treatment or prophylaxis of illnesses which are caused by the binding of adhesive proteins to blood platelets and by blood platelet aggregation and cell-cell adhesion, and are manufactured by cleaving protecting groups in the corresponding protected compounds or by converting the cyano group into the amidino group in corresponding nitriles.
