76421-90-4 Usage
Uses
Used in Research and Analytical Applications:
BIMANE AMINE is used as a fluorescent probe for detecting and measuring primary amines. Its ability to form covalent bonds with primary amines and produce a fluorescent product makes it a valuable tool in various research and analytical applications.
Used in Chemical Synthesis:
BIMANE AMINE can be used as a building block in the synthesis of various fluorescent compounds and conjugates. Its reactivity with primary amines allows for the creation of new molecules with unique properties and potential applications.
Used in Biochemistry and Molecular Biology:
BIMANE AMINE can be used to label and track primary amine-containing biomolecules, such as proteins and peptides, in biological systems. This can provide valuable insights into the structure, function, and interactions of these molecules in living organisms.
Used in Environmental Analysis:
BIMANE AMINE can be employed as a sensor for detecting primary amines in environmental samples, such as water and soil. Its high sensitivity and selectivity for primary amines make it a useful tool for monitoring and assessing the presence of these compounds in the environment.
Used in Pharmaceutical Development:
BIMANE AMINE can be utilized in the development of new drugs and drug delivery systems that target primary amine-containing enzymes, receptors, or other biological targets. Its ability to form covalent bonds with primary amines can be harnessed to improve the efficacy and selectivity of these therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 76421-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,2 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76421-90:
(7*7)+(6*6)+(5*4)+(4*2)+(3*1)+(2*9)+(1*0)=134
134 % 10 = 4
So 76421-90-4 is a valid CAS Registry Number.
76421-90-4Relevant academic research and scientific papers
Bimanes. 6. Reactive halogen derivatives of syn- and anti-1,5-diazabicyclo[3.3.0]octadienediones (9,10-dioxabimanes)
Kosower, Edward M.,Pazhenchevsky, Barak,Dodiuk, Hanna,Kanety, Hannah,Faust, Dov
, p. 1666 - 1673 (2007/10/02)
The preparation of reactive halogen derivatives of syn- and anti-1,5-diazabicyclo[3.3.0]octadienediones (9,10-dioxabimanes) is accomplished through the intermediate monobromo- and dibromobimanes previously described. Mono- and dihydroxy compounds are produced from the bromides by reaction with wet sodium trifluoroacetate in CH3CN and are used to prepare the (a) monochlorides and dichlorides (SOCl2) and (b) the monofluorides and difluorides (Et2NSF3). Monofunctional halides react with nucleophiles (amines, thiols, carboxylates) to yield direct substitution products, with some reduction accompanying the thiol reaction. Difunctional halides react with excess nucleophile to give direct disubstitution products. syn-Dihalides react with difunctional nucleophiles (actual or potential, e.g., RNH2, S2-, (CN)2C2,CH3)B are markedly affected by the nature of X. Most syn-bromobimanes are nonfluorescent and are moderately photosensitive, due to thermally reversible isomerizations and additional irreversible reactions. syra-Chlorobimanes are nonfluorescent to weakly fluorescent. syn-Monofluoro- and difluorobimanes are strongly fluorescent. At 77 K, the halogenated compounds are all phosphorescent to some extent and many of the syn derivatives are strongly fluorescent.
