50398-29-3 Usage
Uses
Used in Chemical Synthesis:
Methanol, bromois used as a precursor in the synthesis of various organic compounds. Its reactivity allows for the formation of a wide range of products, making it a valuable intermediate in the chemical industry.
Used in Pharmaceutical Production:
In the pharmaceutical industry, methanol, bromois utilized in the production of certain medications. Its properties enable it to be a key component in the synthesis of specific drug molecules.
Used in Dye Manufacturing:
Methanol, bromois employed in the manufacturing process of dyes due to its ability to act as a solvent or reactant in dye synthesis, contributing to the coloration and stability of the final product.
Used in Pesticide Production:
In agriculture, methanol, bromois used in the manufacturing of pesticides. Its chemical properties make it suitable for the development of effective pest control agents.
Used as a Flame-Retardant:
Methanol, bromois utilized as a flame-retardant in various applications to reduce the flammability of materials, enhancing safety in industries where fire hazards are a concern.
Check Digit Verification of cas no
The CAS Registry Mumber 50398-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,9 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50398-29:
(7*5)+(6*0)+(5*3)+(4*9)+(3*8)+(2*2)+(1*9)=123
123 % 10 = 3
So 50398-29-3 is a valid CAS Registry Number.
50398-29-3Relevant academic research and scientific papers
An expeditious and efficient bromomethylation of thiols: Enabling bromomethyl sulfides as useful building blocks
Silva-Cuevas, Carolina,Paleo, Ehecatl,León-Rayo, David F.,Lujan-Montelongo, J. Armando
, p. 24654 - 24659 (2018/07/25)
A facile and highly efficient method for the bromomethylation of thiols, using paraformaldehyde and HBr/AcOH, has been developed, which advantageously minimizes the generation of highly toxic byproducts. The preparation of 22 structurally diverse α-bromomethyl sulfides illustrates the chemo-tolerant applicability while bromo-lithium exchange and functionalization sequences, free radical reductions, and additions of the title compounds demonstrate their synthetic utility.
Clean, high-yield preparation of S,S and R,S amino acid isosteres
-
, (2008/06/13)
The present invention provides compounds and methods that can be used to convert the intermediate halomethyl ketones (HMKs), e.g., chloromethyl ketones, to the corresponding S,S- and R,S-diastereomers. More particularly, the present invention provides: (1) reduction methods; (2) inversion methods; and (3) methods involving the epoxidation of alkenes. Using the various methods of the present invention, the R,S-epoxide and the intermediary compounds can be prepared reliably, in high yields and in high purity.
