2198-66-5 Usage
Description
2-BROMO-4-TERT-BUTYLPHENOL is a white crystalline synthetic compound with the chemical formula C10H13BrO. It is characterized by the presence of a bromine atom at the 2nd position and a tert-butyl group at the 4th position on a phenol ring. 2-BROMO-4-TERT-BUTYLPHENOL is known for its unique chemical properties and potential applications in various industries.
Uses
Used in Chemical Synthesis:
2-BROMO-4-TERT-BUTYLPHENOL is used as a key intermediate in the synthesis of various organic compounds. It serves as a building block for the preparation of more complex molecules with diverse applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-BROMO-4-TERT-BUTYLPHENOL is used as a starting material for the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Polymer Industry:
2-BROMO-4-TERT-BUTYLPHENOL is used as a monomer in the polymer industry. It can be polymerized to form polymers with specific properties, such as heat resistance, chemical stability, and mechanical strength.
Used in Agrochemical Industry:
In the agrochemical industry, 2-BROMO-4-TERT-BUTYLPHENOL is used as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its unique structure contributes to the development of effective and environmentally friendly products.
Used in Dye and Pigment Industry:
2-BROMO-4-TERT-BUTYLPHENOL is used as a starting material for the synthesis of dyes and pigments. Its chemical properties allow for the creation of vibrant colors and stable pigments for various applications, such as textiles, plastics, and coatings.
Used in Flavor and Fragrance Industry:
In the flavor and fragrance industry, 2-BROMO-4-TERT-BUTYLPHENOL is used as a building block for the synthesis of various aroma compounds. Its unique structure contributes to the development of new and innovative fragrances and flavors.
Overall, 2-BROMO-4-TERT-BUTYLPHENOL is a versatile synthetic compound with a wide range of applications across different industries. Its unique chemical properties and potential for further synthesis make it a valuable asset in the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 2198-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,9 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2198-66:
(6*2)+(5*1)+(4*9)+(3*8)+(2*6)+(1*6)=95
95 % 10 = 5
So 2198-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BrO/c1-10(2,3)7-4-5-9(12)8(11)6-7/h4-6,12H,1-3H3
2198-66-5Relevant articles and documents
Selective metalation of phenol-type proligands for preparative organometallic chemistry
Berkefeld, Andreas,Fr?hlich, Markus,Kordan, Mike,H?rner, Gerald,Schubert, Hartmut
, p. 3987 - 3990 (2020)
The selective C-metalation of phenol ester derived proligands is a readily applicable addition to state-of-the-art protocols toward cyclometalated structures, in particular of the base metals. The approach is demonstrated by the ortho-nickelation of a 1,10-phenanthroline based strong-field ligand platform that is a sought-after motif in the field of base-metal photochemistry.
Selective Bromination of β-Positions of Porphyrin by Self-Catalytic Behaviour of VOTPP: Facile Synthesis, Electrochemical Redox Properties and Catalytic Application
Maurya, Mannar R.,Prakash, Ved,Avecilla, Fernando,Sankar, Muniappan
, p. 1685 - 1694 (2021/05/03)
Oxidovanadium(IV) complex of β-octabromo-meso-tetraphenylporphyrin, {[VIVO(TPPBr8)], 2} was synthesized by self-catalytic oxidative bromination of meso-tetraphenylporphyrinatooxidovanadium(IV) {[VIVO(TPP), 1} in excellent yield under mild conditions at 25 °C and its structure was confirmed by single crystal X-ray study. UV-Vis and 1H NMR spectra further confirmed that the meso-phenyl rings are not brominated and thus emphasizes on the selectivity as well as synthetic importance of this catalytic method. In the presence of substrates e. g. phenol derivatives, 1 biomimics the vanadium bromoperoxidase (VBPO) enzyme and catalyses the oxidative bromination of substrates in water at 25 °C. Remarkably, 2 also catalyses the oxidative bromination of phenol derivatives under similar reaction conditions with very high turnover frequency (TOF) values (ca. 29 s?1) along with its recyclability. It was found that 2 showed superior catalytic performance as compared to 1 because of its electron deficient nature due to electron withdrawing bromo substituents and robust saddle shaped nonplanar structure (further supported by DFT studies).
Regioselective monobromination of phenols with KBr and ZnAl–BrO3?–layered double hydroxides
Wang, Ligeng,Feng, Chun,Zhang, Yan,Hu, Jun
supporting information, (2020/02/22)
The regioselective mono-bromination of phenols has been successfully developed with KBr and ZnAl–BrO3?–layered double hydroxides (abbreviated as ZnAl–BrO3?–LDHs) as brominating reagents. The para site is much favorable and the ortho site takes the priority if para site is occupied. This reaction featured with excellent regioselectivity, cheap brominating reagents, mild reaction condition, high atom economy, broad substrate scope, and provided an efficient method to synthesize bromophenols.