76102-92-6 Usage
General Description
2-amino-N-(3-pyridinyl)benzamide is a chemical compound with the molecular formula C12H11N3O. 2-amino-N-(3-pyridinyl)benzamide belongs to the class of organic compounds known as benzoylureas, which are organic compounds containing a urea derivative with a structure consisting of a benzoyl group attached to the N-H of a carbamate. It is used in the synthesis of various pharmaceuticals and can also act as an intermediate for the production of other chemicals. 2-amino-N-(3-pyridinyl)benzamide is a solid with a white to light yellow color and is sparingly soluble in water. It is important to handle this compound with caution as it can cause irritation to the skin, eyes, and respiratory system upon contact.
Check Digit Verification of cas no
The CAS Registry Mumber 76102-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,0 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76102-92:
(7*7)+(6*6)+(5*1)+(4*0)+(3*2)+(2*9)+(1*2)=116
116 % 10 = 6
So 76102-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H11N3O/c13-11-6-2-1-5-10(11)12(16)15-9-4-3-7-14-8-9/h1-8H,13H2,(H,15,16)
76102-92-6Relevant articles and documents
MODIFIED PROTEINS AND PROTEIN DEGRADERS
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Paragraph 00919-00921, (2021/12/08)
Provided herein are compounds, pharmaceutical compositions, and methods for binding or degrading target proteins. Further provided herein are compounds having a DNA damage-binding protein 1 (DDB1) binding moiety. Some such embodiments include a linker. Some such embodiments include a target protein binding moiety. Further provided herein are ligand-DDB1 complexes. Further provided herein are in vivo modified DDB1 proteins.
Sulfur-Promoted Synthesis of 2-Aroylquinazolin-4(3H)-ones by Oxidative Condensation of Anthranilamide and Acetophenones
Nguyen, Thanh Binh,Hou, Jing-ya,Retailleau, Pascal
, p. 3337 - 3341 (2019/06/13)
A sulfur-promoted three-component reaction of isatoic anhydride, primary aliphatic or aromatic amines, and acetophenones leading to densely substituted 3-substituted 2-aroylquinazolin-4(3H)-ones is reported. The key step involves a cascade reaction of selective oxidation of the methyl group of the acetophenones, followed by a condensation with anthranilamides. The scope of the reaction is applicable to the synthesis of tryptanthrin and various 3-unsubstituted 2-aroylquinazolin-4(3H)-ones. (Figure presented.).
