57013-94-2 Usage
Description
[1,1'-Biphenyl]-3-amine, 4-chloro-, also known as 4-chloro-1,1'-biphenyl-3-amine, is a chemical compound with the molecular formula C12H10ClN. It is a biphenyl derivative featuring an amino group and a chlorine atom attached to the 4th position of one of the benzene rings. [1,1'-Biphenyl]-3-amine, 4-chlorois recognized for its diverse reactivity and ability to undergo various chemical transformations, making it a versatile and useful compound in organic synthesis.
Uses
Used in Pharmaceutical Synthesis:
[1,1'-Biphenyl]-3-amine, 4-chlorois used as a building block in the synthesis of various pharmaceuticals and organic compounds. Its unique structural features allow it to be a key component in the development of new drugs and medications.
Used in Dye and Pigment Production:
[1,1'-Biphenyl]-3-amine, 4-chlorois also utilized in the production of dyes, pigments, and other organic chemicals, where its chemical properties contribute to the color and stability of the final products.
Used in Material Science and Research:
[1,1'-Biphenyl]-3-amine, 4-chlorohas potential applications in material science and research as a building block for the development of new materials and compounds. Its structural versatility and reactivity make it a valuable asset in the creation of innovative materials with specific properties for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 57013-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,1 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57013-94:
(7*5)+(6*7)+(5*0)+(4*1)+(3*3)+(2*9)+(1*4)=112
112 % 10 = 2
So 57013-94-2 is a valid CAS Registry Number.
57013-94-2Relevant articles and documents
Catalyst-Controlled Regioselective Chlorination of Phenols and Anilines through a Lewis Basic Selenoether Catalyst
Dinh, Andrew N.,Maddox, Sean M.,Vaidya, Sagar D.,Saputra, Mirza A.,Nalbandian, Christopher J.,Gustafson, Jeffrey L.
, p. 13895 - 13905 (2020)
We report a highly efficient ortho-selective electrophilic chlorination of phenols utilizing a Lewis basic selenoether catalyst. The selenoether catalyst resulted in comparable selectivities to our previously reported bis-thiourea ortho-selective catalyst, with a catalyst loading as low as 1%. The new catalytic system also allowed us to extend this chemistry to obtain excellent ortho-selectivities for unprotected anilines. The selectivities of this reaction are up to >20:1 ortho/para, while the innate selectivities for phenols and anilines are approximately 1:4 ortho/para. A series of preliminary studies revealed that the substrates require a hydrogen-bonding moiety for selectivity.
