57858-24-9 Usage
Uses
Used in Organic Synthesis:
BROMOACETIC-1-13C ACID is used as a building block for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with different properties and applications.
Used in Research Applications:
BROMOACETIC-1-13C ACID is used as a research tool for studying the function and inhibition of carbonic anhydrase B in human erythrocytes. This helps researchers understand the enzyme's role in various biological processes and develop potential therapeutic strategies for related conditions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, BROMOACETIC-1-13C ACID is used as a starting material for the development of new drugs. Its alkylating properties make it a valuable component in the synthesis of various pharmaceutical compounds, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Analysis:
BROMOACETIC-1-13C ACID can be employed in chemical analysis to study the interactions between molecules and their environments. The presence of the carbon-13 isotope allows for the use of advanced analytical techniques, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy, to gain insights into molecular structures and properties.
Used in Environmental Science:
BROMOACETIC-1-13C ACID can be utilized in environmental science to study the fate and transport of pollutants in the environment. The stable isotope labeling enables the tracking of specific compounds and their interactions with various environmental matrices, providing valuable information for the development of effective pollution control strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 57858-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,5 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57858-24:
(7*5)+(6*7)+(5*8)+(4*5)+(3*8)+(2*2)+(1*4)=169
169 % 10 = 9
So 57858-24-9 is a valid CAS Registry Number.
57858-24-9Relevant academic research and scientific papers
Leete, Edward,Yu, Ming-Li
, p. 1093 - 1098 (1980)
DL-Ornithine-2> was synthesized from acetate- and ethyl acetamidocyanoacetate.This labelled material was mixed with DL-ornithine- and fed to Nicotiana glutinosa plants by the wick method.After 10 days the plants were harvested affording radioactive nicotine and nornicotine (0.14percent and 0.051percent specific incorporations, respectively).Even at these low specific incorporations an examination of their 13C NMR spectra established the incorporation of ornithine symmetrically into the pyrrolidine rings of these alkaloids.Satellites were observable at the signals due to C-2'. 3', 4' and 5' positions, arising by the presence of contiguous carbons at C-2', 3' and C-4', 5'. - Key Word Index: Nicotiana glutinosa; Solanaceae; nicotine; nornicotine; ornithine; 13C NMR spectroscopy; biosynthesis.
Generation of [β-(phenylsulfonyl)alkylidene]carbenes from hypervalent alkenyl- and alkynyliodonium tetrafluoroborates and synthesis of 1-(phenylsulfonyl)cyclopentenes
Ochiai, Masahito,Kunishima, Munetaka,Tani, Shohei,Nagao, Yoshimitsu
, p. 3135 - 3142 (2007/10/02)
Michael-type addition of benzenesulfinic acid to alkynyl(phenyl)iodonium tetrafluoroborates in methanol gives stereoselectively (Z)-(β-(phenylsulfonyl)alkenyl)iodonium tetrafluoroborates in high yields. [β-(Phenylsulfonyl)alkylidene]carbenes derived from
Transacylation of Cephalosporin; Isolation and Reactions of the Imidate Esters
Saito, Toshinori,Nishihata, ken,Fukatsu, Syunzo
, p. 1058 - 1063 (2007/10/02)
The reaction of the imidate ester of methyl 7-acetamidoceph-3-em-4-carboxylate (2) and phenylacetyl chloride was followed by 13C n.m.r. spectroscopy, which disclosed the intermediacy of the adduct of (2) with the acyl chloride.Transacylations of methyl 7-
