15378-31-1 Usage
Uses
Used in Pharmaceutical Industry:
3-bromo-2-(bromomethyl)prop-1-ene is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds, contributing to the development of new treatments and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 3-bromo-2-(bromomethyl)prop-1-ene serves as an essential intermediate for the production of various agrochemicals. Its properties enable the synthesis of compounds that can be used in pest control and crop protection, thereby supporting agricultural productivity.
Used as a Solvent:
3-bromo-2-(bromomethyl)prop-1-ene can also function as a solvent in certain chemical processes. Its ability to dissolve a variety of substances makes it a valuable component in specific applications within the chemical industry.
Used in Organic Synthesis:
3-broMo-2-(broMoMethy)prop-1-ene is employed in the synthesis of a broad spectrum of organic molecules. Its reactivity and structural features make it a useful building block for creating complex organic compounds in research and industrial settings.
It is crucial to handle 3-bromo-2-(bromomethyl)prop-1-ene with care due to its flammability and potential to cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be taken to mitigate any risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 15378-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,7 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15378-31:
(7*1)+(6*5)+(5*3)+(4*7)+(3*8)+(2*3)+(1*1)=111
111 % 10 = 1
So 15378-31-1 is a valid CAS Registry Number.
15378-31-1Relevant academic research and scientific papers
TRIMETHYLENEMETHANE DIANION EQUIVALENT IN AQUEOUS MEDIUM
Li, Chao-Jun
, p. 517 - 518 (2007/10/02)
Via an indium mediated Barbier-type reaction in aqueous medium, carbonyl compounds react with a trimethylenemethane dianion equivalent to give the corresponding diols.
