175691-91-5 Usage
Uses
Used in Pharmaceutical and Agrochemical Production:
BIPHENYL-3-CARBOTHIOIC ACID AMIDE is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides.
Used in Organic Synthesis:
BIPHENYL-3-CARBOTHIOIC ACID AMIDE is used as a coupling agent in organic synthesis, facilitating the formation of new chemical compounds.
Used in Material Development:
BIPHENYL-3-CARBOTHIOIC ACID AMIDE is used in the development of materials such as liquid crystals and polymers, enhancing their properties and applications.
Used in Anti-corrosion Coatings:
BIPHENYL-3-CARBOTHIOIC ACID AMIDE is used as an ingredient in anti-corrosion coatings, providing protection against corrosion for various surfaces.
Used in Flame Retardants:
BIPHENYL-3-CARBOTHIOIC ACID AMIDE is used in flame retardants, helping to slow down or prevent the spread of fire in various materials.
Used in UV Stabilizers:
BIPHENYL-3-CARBOTHIOIC ACID AMIDE is used in UV stabilizers, protecting materials from the damaging effects of ultraviolet radiation.
Used in Dye and Pigment Synthesis:
BIPHENYL-3-CARBOTHIOIC ACID AMIDE is used in the synthesis of dyes and pigments, creating strong chemical bonds with other compounds to produce vibrant colors.
Check Digit Verification of cas no
The CAS Registry Mumber 175691-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,6,9 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 175691-91:
(8*1)+(7*7)+(6*5)+(5*6)+(4*9)+(3*1)+(2*9)+(1*1)=175
175 % 10 = 5
So 175691-91-5 is a valid CAS Registry Number.
175691-91-5Relevant academic research and scientific papers
Syntheses and selective inhibitory activities of terphenyl-bisamidines for serine proteases
Von Der Saal, Wolfgang,Engh, Richard A.,Eichinger, Andreas,Gabriel, Bernhard,Kucznierz, Ralf,Sauer, Juergen
, p. 73 - 82 (2007/10/02)
Biphenyl nitriles 5a-c, terphenyl dinitriles 11a-d, and naphthalene-bis(benzonitrile) 11e were prepared by palladium-catalyzed cross coupling reactions and subsequently converted to biphenyl amidines 8a-c and bis(benzamidines) 4a-e. Among the biphenyl amidines 8 only the meta-derivative 8b inhibits factor Xa and trypsin (K(i) = 10 μM). The terphenyl bisamidine 4c does not inhibit factor Xa, trypsin, thrombin, and plasmin, while 4a and 4d are almost equipotent inhibitors of theses enzymes (K(i) 1-6 μM), and 4b and 4e are selective for trypsin (K(i) = 0.2 and 0.3 μM; but K(i) > 1 μM for factor Xa, thrombin, and plasmin). X-ray analysis of crystals of 4b complexed with bovine trypsin revealed a unique binding mode: one benzamidino group binds in the S1 site to the side chain carboxylate of Arg 189. The central phenyl group is twisted away from the S2/S3 sites and the second amidino group contacts the Asn 143 side chain.
