57188-74-6 Usage
Uses
Used in Resin and Plastic Production:
(1-Isopropyl-propa-1,2-dienyl)-Benzene is used as a key component in the production of resins and plastics. Its chemical structure allows it to be polymerized or copolymerized with other monomers, resulting in the formation of various types of resins and plastics with specific properties.
Used in Organic Compound Synthesis:
(1-Isopropyl-propa-1,2-dienyl)-Benzene serves as a chemical intermediate in the synthesis of other organic compounds. Its reactive double bonds and isopropyl group make it a valuable building block for the creation of a wide range of organic molecules.
Used in Solvent Applications:
Due to its solubility properties, (1-Isopropyl-propa-1,2-dienyl)-Benzene is used as a solvent in various chemical processes. It can dissolve a wide range of substances, making it useful in industries such as paint, coatings, and adhesives.
Used in Dye Manufacturing:
(1-Isopropyl-propa-1,2-dienyl)-Benzene is used as a chemical intermediate in the manufacturing of dyes. Its ability to react with other compounds allows for the production of a variety of dyes with different colors and properties.
Used in Pharmaceutical Production:
(1-Isopropyl-propa-1,2-dienyl)-Benzene plays a role in the synthesis of pharmaceuticals, as it can be used to create active pharmaceutical ingredients or serve as a building block for more complex drug molecules.
Used in Agricultural Product Manufacturing:
(1-ISOPROPYL-PROPA-1,2-DIENYL)-BENZENE is also utilized in the production of agricultural products, such as pesticides and herbicides. Its chemical properties make it suitable for use in the development of effective and targeted agrochemicals.
It is important to handle (1-Isopropyl-propa-1,2-dienyl)-Benzene with care due to its potential health hazards, and it should be stored and used in accordance with safety guidelines and regulations.
Check Digit Verification of cas no
The CAS Registry Mumber 57188-74-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,8 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57188-74:
(7*5)+(6*7)+(5*1)+(4*8)+(3*8)+(2*7)+(1*4)=156
156 % 10 = 6
So 57188-74-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H14/c1-4-12(10(2)3)11-8-6-5-7-9-11/h5-10H,1H2,2-3H3
57188-74-6Relevant academic research and scientific papers
Chlorination of phenylallene derivatives with 1-chloro-1,2-benziodoxol-3-one: Synthesis of vicinal-dichlorides and chlorodienes
Zhao, Zhensheng,Murphy, Graham K.
, p. 796 - 802 (2018/04/16)
Allyl and vinyl chlorides represent important structural motifs in organic chemistry. Herein is described the chemoselective and regioselective reaction of aryl- and α-substituted phenylallenes with the hypervalent iodine (HVI) reagent 1-chloro-1,2-benz-iodoxol-3-one. The reaction typically results in vicinal dichlorides, except with proton-containing α-alkyl substituents, which instead give chlorinated dienes as the major product. Experimental evidence suggests that a radical mechanism is involved.
Fluorinative Rearrangements of Substituted Phenylallenes Mediated by (Difluoroiodo)toluene: Synthesis of α-(Difluoromethyl)styrenes
Zhao, Zhensheng,Racicot, Léanne,Murphy, Graham K.
, p. 11620 - 11623 (2017/09/11)
Phenylallenes undergo fluorinative rearrangement upon the action of (difluoroiodo)toluene in the presence of 20 mol % BF3?OEt2 to yield α-difluoromethyl styrenes. This unprecedented reaction was entirely chemoselective for the internal allene π bond, and showed remarkable regioselectivity during the fluorination event. Substituted phenylallenes, phenylallenes possessing both phenyl- and α-allenyl substituents, and diphenylallenes were investigated, and good functional-group compatibility was observed throughout. The ease with which allenes can be prepared on a large scale, and the operational simplicity of this reaction allowed us to rapidly access fluorine-containing building blocks that have not been accessed by conventional deoxyfluorination strategies.
Catalytic enantioselective protoboration of disubstituted allenes. Access to alkenylboron compounds in high enantiomeric purity
Jang, Hwanjong,Jung, Byunghyuck,Hoveyda, Amir H.
supporting information, p. 4658 - 4661 (2015/02/19)
Proto-boryl additions to 1,1-disubstituted allenes in the presence of 1.0-5.0 mol % of chiral NHC-Cu complexes, B2(pin)2, and t-BuOH proceed to afford alkenyl-B(pin) products in up to 98% yield, >98:2 site selectivity, and 98:2 er. T
