82006-84-6 Usage
Description
(3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid is an organic compound with the molecular formula C6H12FNO2. It is a derivative of the amino acid lysine, featuring an added fluoromethyl group and a double bond in the carbon chain. (3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid is not naturally occurring and is typically synthesized in laboratory settings. Its unique structure and potential biological activities make it a candidate for chemical research and pharmaceutical development. However, further research is required to fully understand its properties and potential uses.
Uses
Used in Chemical Research:
(3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid is used as a research compound for studying its chemical properties and reactivity. Its unique structure allows scientists to explore new reactions and mechanisms that could lead to the development of novel chemical processes.
Used in Pharmaceutical Development:
(3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid is used as a starting material or intermediate in the synthesis of new pharmaceutical compounds. Its potential biological activities and unique structure make it a promising candidate for the development of new drugs, particularly in areas where existing treatments are limited or ineffective.
Used in Drug Design:
(3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid is used as a structural component in drug design, where its fluoromethyl group and double bond may confer specific properties to the resulting drug molecules. This can lead to the creation of new drugs with improved pharmacokinetics, selectivity, and efficacy.
Used in Biochemical Studies:
(3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid is used in biochemical studies to investigate its interactions with biological systems. Understanding how this compound interacts with enzymes, receptors, or other biomolecules can provide insights into its potential therapeutic applications and mechanisms of action.
Note: The specific applications and industries for (3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid are not explicitly mentioned in the provided materials. The uses listed above are inferred based on the compound's potential properties and typical applications of similar organic compounds in the fields of chemical research and pharmaceutical development.
Check Digit Verification of cas no
The CAS Registry Mumber 82006-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,0 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82006-84:
(7*8)+(6*2)+(5*0)+(4*0)+(3*6)+(2*8)+(1*4)=106
106 % 10 = 6
So 82006-84-6 is a valid CAS Registry Number.
82006-84-6Relevant articles and documents
A versatile entry into the synthesis of α-(monofluoromethyl) amino acids : Preparation of α-(monofluoromethyl) serine and (E)-dehydro-α-(monofluoromethyl) ornithine
Van Hijfte, Luc,Heydt, Veronique,Kolb, Michael
, p. 4793 - 4796 (2007/10/02)
A new entry to the synthesis of α-(monofluoromethyl) amino acids is described. The synthesis is based on a Strecker reaction on an α-(monofluoromethyl) ketone. As an example, α-(monofluoromethyl) serine was synthesized and used as starting material for a new synthesis of (E)-dehydro-α-(monoflouromethyl) ornithine.
Method of inhibiting the growth of protozoa
-
, (2008/06/13)
α-Substituted amines and α-substituted-α-amino acids are described which are useful in inhibiting the growth of protozoa in animals.
