540495-28-1 Usage
Uses
Used in Pharmaceutical Industry:
Phenol, 3-bromo-4-ethyl(9CI) is utilized as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure and reactivity facilitate the creation of complex molecules with potential medicinal applications.
Used in Agrochemical Industry:
In the agrochemical sector, Phenol, 3-bromo-4-ethyl(9CI) serves as a precursor for the production of various agrochemicals, including pesticides and herbicides. Its chemical properties allow for the design of effective compounds that can protect crops and enhance agricultural productivity.
Used in Materials Science:
Phenol, 3-bromo-4-ethyl(9CI) is employed in materials science for the development of novel materials with specific properties. Its versatility in chemical reactions enables the synthesis of materials with tailored characteristics for use in various applications, such as coatings, adhesives, and polymers.
Used as a Reagent in Organic Chemistry:
Phenol, 3-bromo-4-ethyl(9CI) also finds application as a reagent in organic chemistry reactions. Its unique properties make it suitable for the preparation of complex molecules and the advancement of synthetic methodologies in organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 540495-28-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,0,4,9 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 540495-28:
(8*5)+(7*4)+(6*0)+(5*4)+(4*9)+(3*5)+(2*2)+(1*8)=151
151 % 10 = 1
So 540495-28-1 is a valid CAS Registry Number.
540495-28-1Relevant articles and documents
KRAS G12D INHIBITORS
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Paragraph 0980, (2021/03/05)
The present invention relates to compounds that inhibit KRas G12D. In particular, the present invention relates to compounds that inhibit the activity of KRas G12D, pharmaceutical compositions comprising the compounds and methods of use therefor.
Electronic effects of ring substituents on triplet benzylic biradicals
Wagner, Peter J.,Wang, Lingling
, p. 645 - 647 (2007/10/03)
UV irradiation of α-(o-alkylphenyl)acetophenones with a methoxy or cyano substituent para to the o-alkyl group of the α-aryl ring has revealed that a methoxy group slightly increases the stereoselectivity but not the quantum yield of indanol formation, whereas a cyano group greatly lowers both diastereoselectivity and quantum efficiency, confirming the likelihood that hydrogen-bonding of the hydroxy group to the α-phenyl ring plays an important role in the cyclization of the photogenerated triplet 1,5-biradical intermediates.
