3128-77-6 Usage
Classification
Isonitrile
Isonitriles are a functional group containing a carbon atom with a bond to a nitrogen atom and a side chain with a strong dipole.
Potential applications
Pharmaceutical and agrochemical industries, material science, and organic synthesis
These industries and fields may benefit from the unique properties of 1,1-Biphenyl,2-isocyano-(9CI) in various chemical reactions and processes.
Extensive study
Limited
1,1-Biphenyl,2-isocyano-(9CI) has not been extensively studied, which means its specific properties and uses are not well-documented.
Unique properties
Potential for interesting and valuable applications
Although not well-documented, the compound may possess unique properties that could make it valuable in certain applications.
Chemical structure
1,1-Biphenyl with an isocyano group at the 2nd position
The compound is derived from a biphenyl structure, with an isocyano group (-CN) attached to the 2nd carbon atom of the biphenyl.
Reactivity
Unknown
Due to limited study, the reactivity of 1,1-Biphenyl,2-isocyano-(9CI) with other chemicals is not well-known.
Stability
Unknown
The stability of the compound under various conditions is not well-documented, which may affect its potential applications.
Toxicity
Unknown
The toxicity of 1,1-Biphenyl,2-isocyano-(9CI) is not well-documented, which is an important factor to consider for its potential use in pharmaceutical and agrochemical industries.
Environmental impact
Unknown
The environmental impact of 1,1-Biphenyl,2-isocyano-(9CI) is not well-documented, which is another important factor to consider for its potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3128-77-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3128-77:
(6*3)+(5*1)+(4*2)+(3*8)+(2*7)+(1*7)=76
76 % 10 = 6
So 3128-77-6 is a valid CAS Registry Number.
3128-77-6Relevant articles and documents
Preparation of 6-Difluoromethylphosphonated Phenanthridines by Visible-Light-Driven Radical Cyclization of 2-Isocyanobiphenyls
Wang, Shuang,Jia, Wen-Liang,Wang, Lin,Liu, Qiang
, p. 6817 - 6821 (2015)
A protocol to obtain a variety of 6-difluoromethylenephosphonated phenanthridines through a radical cyclization process was explored. These reactions, performed with the use of diethyl bromodifluoromethylphosphonate as a radical resource and 2-isocyanobip
4CzIPN-tBu-Catalyzed Proton-Coupled Electron Transfer for Photosynthesis of Phosphorylated N-Heteroaromatics
Liu, Yan,Chen, Xiao-Lan,Li, Xiao-Yun,Zhu, Shan-Shan,Li, Shi-Jun,Song, Yan,Qu, Ling-Bo,Yu, Bing
, p. 964 - 972 (2021/01/12)
2,4,5,6-Tetrakis(3,6-di-tert-butyl-9H-carbazol-9-yl)isophthalonitrile (4CzIPN-tBu) was developed as a photocatalyst for the phosphorus-radical-initiated cascade cyclization reaction of isocyanides. By using 4CzIPN-tBu as catalyst, we developed a visible-light-induced proton-coupled electron transfer strategy for the generation of phosphorus-centered radicals, via which a wide range of phosphorylated phenanthridines, quinolines, and benzothiazoles were successfully constructed.
Direct photoexcitation of benzothiazolines: Acyl radical generation and application to access heterocycles
He, Xiang-Kui,Li, Lei,Lu, Juan,Xuan, Jun,Ye, Hai-Bing
, (2021/11/27)
An acyl radical generation and functionalization strategy through direct photoexcitation of benzothiazolines has been developed. The formed acyl radical species can either be trapped by quinoxalin-2-ones to realize their C(3)-H functionalization or trigger a cascade radical cyclization with isonitriles to synthesise biologically important phenanthridines. The synthetic value of this protocol can be further illustrated by the modification of quinoxalin-2-ones, containing important natural products and drug-based complex molecules.
