87487-96-5 Usage
Uses
Used in Organic Synthesis:
3-AMINO-5-HYDROXY-PENTEN-1 is used as a reagent in organic synthesis for the preparation of various pharmaceuticals and agricultural chemicals. Its unique structural features and chemical properties make it a versatile building block for the creation of a wide range of compounds.
Used in Biosynthesis of Natural Products:
As an intermediate in the biosynthesis of certain natural products, 3-AMINO-5-HYDROXY-PENTEN-1 plays a significant role in the production of bioactive compounds with potential applications in medicine, agriculture, and other industries.
Used in the Development of New Materials and Polymers:
Due to its unique structural characteristics, 3-AMINO-5-HYDROXY-PENTEN-1 has potential applications in the development of new materials and polymers. Its ability to form various chemical bonds and interact with other molecules makes it a promising candidate for the creation of innovative materials with specific properties and functions.
Used in Research and Development:
Despite its relative novelty, ongoing research is exploring the full range of potential uses and implications of 3-AMINO-5-HYDROXY-PENTEN-1 in various fields. Its diverse chemical properties and potential applications make it an interesting subject for further investigation and development, with the aim of discovering new applications and enhancing existing ones.
Check Digit Verification of cas no
The CAS Registry Mumber 87487-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,8 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87487-96:
(7*8)+(6*7)+(5*4)+(4*8)+(3*7)+(2*9)+(1*6)=195
195 % 10 = 5
So 87487-96-5 is a valid CAS Registry Number.
87487-96-5Relevant academic research and scientific papers
Continuous Pd-Catalyzed Carbonylative Cyclization Using Iron Pentacarbonyl as a CO Source
Lopatka, Pavol,Markovi?, Martin,Koó?, Peter,Ley, Steven V.,Gracza, Tibor
, p. 14394 - 14406 (2019/11/11)
This work discloses a continuous flow carbonylation reaction using iron pentacarbonyl as source of CO. The described transformation using this surrogate was designed for use in commonly accessible flow equipment. Optimized conditions were applied to a sca
ELECTROPHILIC OLEFIN HETEROCYCLIZATION IN ORGANIC SYNTHESIS. STEREOSELECTIVE INTRAMOLECULAR AMIDOMERCURATION OF γ-HYDROXY-δ,ε-UNSATURATED URETHANES
Tkahata, Hiroki,Tajima, Mayumi,Banba, Yasunori,Momose, Takefumi
, p. 2550 - 2552 (2007/10/02)
Mercuric acetate driven cyclization of γ-hydroxy-δ,ε-unsaturated urethanes 1a,b proceeded regio- and stereoselectively to afford cis-2-acetoxymercurymethyl-3-hydroxypyrrolidines 2a,b, respectively.These were transformed into the key intermediates for seve
SILYL NITRONATES, NITRILE OXIDES, AND DERIVED 2-ISOXAZOLINES IN ORGANIC SYNTHESIS. FUNCTIONALIZATION OF BUTADIENE, A NOVEL ROUTE TO FURANS AND 2-ISOXAZOLINES AS AN ALTERNATIVE TO ALDOL-TYPE CONDENSATIONS
Das, Nalin B.,Torssell, Kurt B. G.
, p. 2247 - 2254 (2007/10/02)
Mono- and di-addition of silylnitronates and nitrile oxides is a useful procedure for functionalizing butadiene leading to cyano and acyl derivatives.A novel route to 2,5-disubstituted furans is also established.The potential of the method in carbohydrate synthesis is pointed out.The route via 2-isoxazoline is shown to be a useful alternative to aldol-type reactions in organic synthesis. 15a has been studied by X-ray diffraction and shown to be meso form.
