84508-51-0 Usage
Uses
Used in Organic Synthesis:
2-BROMOETHANOL (1,2-13C2) is used as a labeled intermediate for organic synthesis, providing a valuable tool for researchers to study reaction mechanisms, monitor reaction progress, and investigate the behavior of specific isotopes in chemical processes. The presence of 13C isotopes in 2-BROMOETHANOL (1,2-13C2) enables the differentiation of the labeled molecule from its unlabeled counterpart, facilitating the analysis of reaction pathways and the identification of intermediates and products.
Used in Research and Development:
In the field of research and development, 2-BROMOETHANOL (1,2-13C2) serves as a crucial component for the synthesis of various organic compounds and the investigation of their properties. The use of this labeled analogue allows for a better understanding of the structural and functional aspects of synthesized molecules, as well as their interactions with other compounds and biological systems.
Used in Pharmaceutical Industry:
2-BROMOETHANOL (1,2-13C2) is used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of new drugs and drug candidates. The incorporation of 13C isotopes in 2-BROMOETHANOL (1,2-13C2) can aid in the elucidation of drug metabolism pathways, the identification of active pharmaceutical ingredients, and the optimization of drug synthesis processes.
Used in Environmental Studies:
In environmental studies, 2-BROMOETHANOL (1,2-13C2) can be employed as a tracer compound to investigate the fate and transport of organic pollutants in the environment. The use of this labeled analogue allows for the tracking of specific contaminants and the assessment of their impact on ecosystems and human health.
Used in Analytical Chemistry:
2-BROMOETHANOL (1,2-13C2) is used as a reference material in analytical chemistry for the calibration of instruments and the development of new analytical methods. The presence of 13C isotopes in 2-BROMOETHANOL (1,2-13C2) provides a unique signature that can be utilized for the accurate quantification and identification of target analytes in complex samples.
Check Digit Verification of cas no
The CAS Registry Mumber 84508-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,0 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84508-51:
(7*8)+(6*4)+(5*5)+(4*0)+(3*8)+(2*5)+(1*1)=140
140 % 10 = 0
So 84508-51-0 is a valid CAS Registry Number.
84508-51-0Relevant academic research and scientific papers
Cao, Kai,Brailsford, John A.,Bonacorsi, Samuel J.
, p. 526 - 530 (2020)
N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide (EDC) is a carbodiimide coupling reagent commonly used for the preparation of amides from carboxylic acids and amines. Because of initial concerns regarding the genotoxicity of EDC and its use in GMP syntheses at Bristol Myers Squibb, the quantitation of residual EDC and its by-product N-(3-dimethylaminopropyl)-N′-ethylurea (EDU) by liquid chromatography–mass spectrometry (LCMS) impurity analysis was required. These analyses required the use of stable-isotope-labeled EDC and EDU to serve as internal standards. To meet this need, stable-isotope-labeled EDC 9 and EDU 10 were prepared from [1,2-13C2] ethylene glycol and [13C,15N] potassium cyanide in overall yields of 6% and 8%, respectively.
