767-99-7 Usage
Description
trans-2-Phenyl-2-butene is an organic compound that features a phenyl group attached to a butene chain with a trans configuration. It is a minimally functionalized olefin, which makes it a valuable synthetic intermediate in various chemical reactions.
Uses
Used in Chemical Synthesis:
trans-2-Phenyl-2-butene is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to participate in a wide range of chemical reactions, making it a versatile building block in organic chemistry.
Used in Asymmetric Hydrogenation Studies:
In the field of catalysis, trans-2-Phenyl-2-butene is used as a reactant to study asymmetric hydrogenations. This application is particularly relevant for understanding the behavior of minimally functionalized olefins when catalyzed by iridium-containing complexes, which can lead to advancements in enantioselective synthesis and the development of more efficient catalysts.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its potential as a synthetic intermediate, trans-2-Phenyl-2-butene could also be used in the pharmaceutical industry for the synthesis of various drug molecules. Its ability to be modified and incorporated into more complex structures makes it a candidate for the development of new pharmaceutical agents.
Used in Materials Science:
Similarly, trans-2-Phenyl-2-butene could be utilized in materials science for the development of new polymers or materials with specific properties. Its structural characteristics may contribute to the creation of materials with tailored characteristics for various applications, such as in electronics, coatings, or adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 767-99-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 767-99:
(5*7)+(4*6)+(3*7)+(2*9)+(1*9)=107
107 % 10 = 7
So 767-99-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H12/c1-3-9(2)10-7-5-4-6-8-10/h3-8H,1-2H3/b9-3-
767-99-7Relevant articles and documents
Regioselective Three-Component Synthesis of Vicinal Diamines via 1,2-Diamination of Styrenes
Cao, Jie,Lv, Daqi,Yu, Fei,Chiou, Mong-Feng,Li, Yajun,Bao, Hongli
supporting information, p. 3184 - 3189 (2021/05/05)
The vicinal diamine motif plays a significant role in natural products, drug design, and organic synthesis, and development of synthetic methods for the synthesis of diamines is a long-standing interest. Herein, we report a regioselective intermolecular three-component vicinal diamination of styrenes with acetonitrile and azodicarboxylates. The diamination products can be produced in moderate to excellent yields via the Ritter reaction. Synthetic applications and theoretical studies of this reaction have been conducted.
Visible-Light-Induced Meerwein Fluoroarylation of Styrenes
Tang, Hai-Jun,Zhang, Bin,Xue, Fei,Feng, Chao
supporting information, p. 4040 - 4044 (2021/05/26)
An unprecedented approach for assembling a broad range of 1,2-diarylethane derivatives with fluorine-containing fully substituted carbon centers was developed. The protocol features straightforward operation, proceeds under metal-free condition, and accommodates a large variety of synthetically useful functionalities. The critical aspect to the success of this novel transformation lies in using aryldiazonium salts as both aryl radical progenitor and also as single electron acceptor which elegantly enables a radical-polar crossover manifold.
