39220-69-4 Usage
Uses
Used in Organic Synthesis:
1-bromo-4-(1-methylpropyl)benzene is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure, with a bromine atom and a tert-butyl group, allows for versatile reactions and the formation of a wide range of organic products.
Used in Chemical Reactions as a Reagent:
In the chemical industry, 1-bromo-4-(1-methylpropyl)benzene serves as a reagent in numerous chemical reactions. Its reactivity stems from the presence of the bromine atom, which can participate in substitution, addition, and elimination reactions, facilitating the synthesis of desired products.
Used in Pharmaceutical Industry:
1-bromo-4-(1-methylpropyl)benzene is utilized in the pharmaceutical industry as an intermediate for the synthesis of various drugs. Its specific functional groups and structural features make it a valuable component in the development of new medicinal compounds.
Used in Fragrance Industry:
Due to its strong, aromatic odor, 1-bromo-4-(1-methylpropyl)benzene finds application in the fragrance industry as a component in the creation of perfumes, colognes, and other scented products. Its unique scent profile contributes to the overall aroma of these products.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 1-bromo-4-(1-methylpropyl)benzene is employed as an intermediate for the synthesis of various dyes and pigments. Its chemical properties allow for the development of colorants with specific characteristics, such as hue, stability, and solubility.
Used in Polymer Industry:
1-bromo-4-(1-methylpropyl)benzene is also used in the polymer industry as a monomer or a precursor in the synthesis of polymers with specific properties. Its incorporation into polymer chains can influence the material's characteristics, such as thermal stability, mechanical strength, and chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 39220-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,2 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39220-69:
(7*3)+(6*9)+(5*2)+(4*2)+(3*0)+(2*6)+(1*9)=114
114 % 10 = 4
So 39220-69-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H13Br/c1-3-8(2)9-4-6-10(11)7-5-9/h4-8H,3H2,1-2H3
39220-69-4Relevant academic research and scientific papers
Bioinspired Metal-Free Formal Decarbonylation of α-Branched Aliphatic Aldehydes at Ambient Temperature
Richter, Sven C.,Oestreich, Martin
supporting information, p. 8508 - 8512 (2019/06/04)
A sequence of a Baeyer–Villiger oxidation and a Lewis acid-promoted reduction of the resulting formate with Et3SiH enabled the metal-free formal decarbonylation of tertiary and secondary aliphatic aldehydes. The new methodology mimics the biosynthetic decarbonylation pathway through oxidative C?C bond cleavage rather than the C(O)?H bond activation known from conventional Tsuji–Wilkinson-type reactions. The substrate scope is complementary to existing transition-metal-catalyzed protocols.
A Green protocol for the bromination and iodination of the aromatic compounds using H5IO6/NaBr and H5IO 6/NaI in the water
Yousefi-Seyf, Jaber,Tajeian, Kazem,Kolvari, Eskandar,Koukabi, Nadiya,Khazaei, Ardeshir,Zolfigol, Mohammad Ali
, p. 2619 - 2622 (2012/10/29)
Bromination and iodination of the aromatic compounds have efficiently been carried out at room temperature and 70 °C, respectively, in short reaction times using orthoperiodic acid/sodium bromide (1:2) and orthoperiodic acid/sodium iodide (1:2) in water to prepare the corresponding halo compounds with excellent yields.
