6065-79-8 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2,3-dibromopropyl propanoate is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and agricultural products due to its unique chemical structure and reactivity.
Used in Organic Synthesis:
In the realm of organic synthesis, 2,3-dibromopropyl propanoate serves as a reagent for the introduction of bromoalkyl groups, which is crucial for the creation of specific organic compounds and molecules with desired properties.
Used in Insect Repellent and Pesticide Development:
Leveraging its insecticidal properties, 2,3-dibromopropyl propanoate is employed in the formulation of insect repellents and pesticides, providing an effective means to control and prevent infestations in various settings.
Safety Considerations:
Due to the potential harmful effects of 2,3-dibromopropyl propanoate, it is imperative that this chemical is handled and stored with caution, adhering to proper safety protocols to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6065-79-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6065-79:
(6*6)+(5*0)+(4*6)+(3*5)+(2*7)+(1*9)=98
98 % 10 = 8
So 6065-79-8 is a valid CAS Registry Number.
6065-79-8Relevant academic research and scientific papers
Carbon-13 NMR Spectra of Bromine-containing Esters
Velichko, F. K.,Dostovalova, V. I.,Vinogradova, L. V.,Freidlina, R Kh.
, p. 442 - 446 (2007/10/02)
13CHBrCOOR fragments of bromine-containing mono- and dicarboxylates show 13C NMR signals in the range 38-45 ppm, at 12-15 ppm to high field of their chloro analogues.The introduction of one bromine atom into the α-CH2 group causes a 6-13 ppm shift of the carbon signal, depending on the type of ester.The replacement of H with Br in 13C2H2(COOR)2 has only a negligible influence on the 13CH2 signal position.The 13CBr2COOR fragment signals appear in the range 40-54 ppm. 13C NMR data, including the chemical shift values, signal multiplicities and spin-spin couplings, make possible the identification of isomers present in isomer mixtures of bromine-containing esters.The 13COOR chemical shifts of diastereomers of α,β-dibromoesters differ noticeably from each other, and the 13C NMR spectra can thus be used to supply preliminary information about the stereochemistry of bromine addition to α,β-unsaturated acids.
