188665-76-1 Usage
Uses
Used in Pharmaceutical Research:
[1,1'-Biphenyl]-3-carboxamide is used as a compound in pharmaceutical research for its various biological activities, including anti-tumor, anti-inflammatory, and anti-fungal properties. Its versatile nature makes it a promising candidate for drug development.
Used in Organic Synthesis:
In the field of organic synthesis, [1,1'-Biphenyl]-3-carboxamide is used as a key intermediate or building block for the synthesis of more complex molecules, leveraging its unique chemical structure and reactivity.
Used in Drug Development:
[1,1'-Biphenyl]-3-carboxamide is used as a potential drug candidate due to its demonstrated biological activities. Its anti-tumor properties, in particular, make it a valuable compound for the development of new therapeutic agents against cancer.
Used in Medicinal Chemistry:
In medicinal chemistry, [1,1'-Biphenyl]-3-carboxamide is used as a versatile compound for the design and synthesis of novel drugs. Its chemical structure allows for modifications and functionalization, enabling the development of new molecules with improved pharmacological properties.
Overall, [1,1'-Biphenyl]-3-carboxamide is a valuable compound in the fields of pharmaceutical research, organic synthesis, drug development, and medicinal chemistry, thanks to its diverse biological activities and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 188665-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,6,6 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 188665-76:
(8*1)+(7*8)+(6*8)+(5*6)+(4*6)+(3*5)+(2*7)+(1*6)=201
201 % 10 = 1
So 188665-76-1 is a valid CAS Registry Number.
188665-76-1Relevant academic research and scientific papers
Rh(III)-Catalyzed Redox-Neutral Annulation of Primary Benzamides with Diazo Compounds: Approach to Isoquinolinones
Wu, Youzhi,Sun, Peng,Zhang, Kaifan,Yang, Tie,Yao, Hequan,Lin, Aijun
, p. 2166 - 2173 (2016/03/15)
Reported herein is a Rh-catalyzed redox-neutral annulation of primary benzamides with diazo compounds, representing an efficient and economic protocol to isoquinolinones. The procedure exhibited good functional group tolerability, scalability, and regioselectivity, obviating the need for oxidants, and only environmentally benign N2 and H2O were released. Further utilization of the method provided an alternative route to functionalized isoquinolines.
BLUE LUMINESCENT COMPOUNDS
-
, (2013/10/22)
There is provided a compound having Formula (I). In the formula: R1 can be alkyl, aryl, alkylaryl, or deuterated analogs thereof; R2 can be alkyl or deuterated alkyl; R3 can be H, D, aryl, or deuterated aryl; and R4-R6 are the same or different and can be H, D, alkyl, or deuterated alkyl. In the formula, at least one of the following conditions is met: (i) R1 is a secondary alkyl, a tertiary alkyl, aryl, alkylaryl, or deuterated analog thereof; (ii) R3 is aryl or deuterated aryl; (iii) at least one of R3-R6 is D.
The formation of dicyanoterphenyls by the interaction of terephthalonitrile dianion with biphenylcarbonitriles in liquid ammonia
Panteleeva, Elena V.,Bagryanskaya, Irina Yu.,Sal'Nikov, Georgij E.,Shteingartsa, Vitalij D.
experimental part, p. 123 - 133 (2011/06/23)
Terephthalonitrile dianion couples with biphenylcarbonitriles providing dicyanosubstituted m- and p-terphenyls. The influence of the cyano group position in biphenylcarbonitrile on the structure of the terphenyl scaffold is discussed. ARKAT USA, Inc.
