50553-14-5 Usage
Description
2,3-Dibromobutanal is a chemical compound characterized by the molecular formula C4H6Br2O. It presents as a colorless to pale yellow liquid with a distinct pungent odor. 2,3-Dibromobutanal is recognized for its role as an intermediate in the synthesis of various products, particularly in the pharmaceutical and agrochemical industries. Its utility extends to organic synthesis as a reagent and as a solvent in chemical reactions, highlighting its versatility in chemical processes.
Uses
Used in Pharmaceutical Synthesis:
2,3-Dibromobutanal is utilized as an intermediate in the production of pharmaceuticals, contributing to the development of new medications and therapeutic agents. Its chemical properties make it a valuable component in the synthesis of complex organic molecules.
Used in Agrochemical Production:
In the agrochemical industry, 2,3-Dibromobutanal serves a similar role as an intermediate, aiding in the creation of compounds used in agricultural applications such as pesticides and herbicides, which are essential for crop protection and yield enhancement.
Used as a Reagent in Organic Synthesis:
2,3-Dibromobutanal is employed as a reagent in organic synthesis, facilitating various chemical reactions that lead to the formation of desired organic compounds. Its reactivity and stability make it suitable for use in a range of organic chemical processes.
Used as a Solvent in Chemical Reactions:
Additionally, 2,3-Dibromobutanal functions as a solvent in chemical reactions, providing a medium for reactions to occur. Its properties allow it to dissolve a variety of substances, making it a useful component in many chemical processes.
Safety Considerations:
Given its highly flammable nature and potential for violent reactions with oxidizing agents, 2,3-Dibromobutanal requires careful handling and storage to prevent accidents. Moreover, exposure to this chemical may result in irritation to the eyes, skin, and respiratory system, necessitating the use of appropriate protective measures when working with it.
Check Digit Verification of cas no
The CAS Registry Mumber 50553-14-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,5 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50553-14:
(7*5)+(6*0)+(5*5)+(4*5)+(3*3)+(2*1)+(1*4)=95
95 % 10 = 5
So 50553-14-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H6Br2O/c1-3(5)4(6)2-7/h2-4H,1H3
50553-14-5Relevant articles and documents
N-Heterocyclic Carbene-Catalyzed β-Indolylation of α-Bromoenals with Indoles
Sun, Shaofa,Lang, Ming,Wang, Jian
supporting information, p. 5704 - 5708 (2019/12/24)
An unprecedented example of NHC-catalyzed β-indolylation of α-bromoenals with indoles has been developed. This concise protocol features several advantages (mild reaction conditions, broad substrate scope) and constructs synthetically useful building blocks, namely β-biaryl methylene esters. Notably, the β-biaryl methylene-type fragment is widely found in natural products or pharmaceuticals. (Figure presented.).
Studies towards total synthesis of antillatoxin: Investigation of the indium-mediated allylation reactions of carbonyl compounds with β-bromocrotylbromide in water
Loh, Teck-Peng,Cao, Guo-Qiang,Pei, Jian
, p. 1453 - 1456 (2007/10/03)
Indium mediates the coupling of β-bromocrotylbromide with carbonyl compounds in saturated ammonium chloride in the presence of lanthanide triflate under sonication to give the corresponding compounds in good yield and moderate to high syn diastereoselecti
