((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one

Base Information

  • Chemical Name: ((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one
  • CAS No.: 79200-56-9

Quality products?make an important contribution to long-term revenue and profitability. Manufacturer supply top purity ((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one 79200-56-9 with GMP standards

1.What is the ((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one ?

((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one is a bicyclic organic compound with a unique structure and versatile applications in the pharmaceutical industry. It is characterized by its specific stereochemistry, with the R configuration at the first carbon and the S configuration at the fourth carbon, which contributes to its distinct properties and reactivity.

2.What is the CAS number for ((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one ?

The CAS number of ((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one is 79200-56-9.

3.What are another words for ((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one ?

Synonyms?for?((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one 79200-56-9:(1R,4S)-(-)-2-Azabicyclo[2.2.1]hept-5-en-3-one;

4.What is ((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one (79200-56-9) used for?

(1R)-(-)-2-Azabicyclo[2.2.1]hept-5-en-3-one can be used as a precursor to prepare: Amino-peramivir, a potent neuraminidase inhibitor.Five membered analogs of 4-amino-5-halopentanoic acids as potential GABA aminotransferase (GABA-AT) inactivators.

InChI:InChI=1/C6H7NO/c8-6-4-1-2-5(3-4)7-6/h1-2,4-5H,3H2,(H,7,8)/t4-,5+/m1/s1

Relevant articles related to ((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one:

Article

Source

Chemical preparation method of 2-azabicyclo [2.2.1] hept-5-ene-3-one with optical activity

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Yin, Jin-Gang,Gong, Yi,Zhang, Xiao-Yan,Zheng, Gao-Wei,Xu, Jian-He

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Enhanced enzymatic synthesis of the enantiopure intermediate for the blockbuster drug intermediate abacavir through a two-step enzymatic cascade reaction

Galla, Zsolt,Forró, Enik?,Fül?p, Ferenc

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5.Buy ((1R,4S)-2-Azabicyclo[2.2.1]hept-5-en-3-one with the best price .

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