125772-44-3 Usage
Uses
Used in Organic Synthesis:
BIPHENYL-4-CARBOXAMIDINE is used as a building block in organic synthesis for its versatile chemical properties, allowing for the creation of a wide range of complex organic compounds.
Used in Chemical Reactions:
It serves as a reagent in various chemical reactions, facilitating the formation of desired products and contributing to the advancement of chemical research and development.
Used in Pharmaceutical Production:
BIPHENYL-4-CARBOXAMIDINE is utilized in the production of pharmaceuticals due to its potential as a pharmacologically active molecule, playing a crucial role in the development of new drugs.
Used in Agrochemical Production:
It is also employed in the manufacturing of agrochemicals, where its chemical properties contribute to the effectiveness of these products in agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 125772-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,7,7 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 125772-44:
(8*1)+(7*2)+(6*5)+(5*7)+(4*7)+(3*2)+(2*4)+(1*4)=133
133 % 10 = 3
So 125772-44-3 is a valid CAS Registry Number.
125772-44-3Relevant academic research and scientific papers
Direct Conversion of Amidoximes to Amidines via Transfer Hydrogenation
Anbazhagan, Mariappan,Boykin, David W.,Stephens, Chad E.
, p. 2467 - 2469 (2007/10/03)
Amidoximes, O-alkylamidoximes, and O-acylamidoximes are directly converted to amidines by reaction with ammonium formate and Pd/C in acetic acid.
Photochemistry of crystalline chlorodiazirines: The influence of conformational disorder and intermolecular Cl...N=N interactions on the solid-state reactivity of singlet chlorocarbenes
Sanrame, Carlos N.,Suhrada, Christopher P.,Dang, Hung,Garcia-Garibay, Miguel A.
, p. 3287 - 3294 (2007/10/03)
A photochemical study was carried out with 3-substituted 3-chlorodiazirines with 4-biphenyl- (4a), (4-biphenyl)methyl- (4b), 2-(4-biphenyl)ethyl- (4c), and 1,1-dimethyl-1-(4-biphenyl)methyl (4d) substitueras. The chlorodiazirines were prepared from the co
