122624-72-0 Usage
Description
(+/-)-cis-(4-hydroxymethyl)cyclopent-2-en-1-ylamine is a chiral amine chemical compound that features a cyclopentene ring with a hydroxymethyl group attached to it. It is commonly utilized in organic synthesis and medicinal chemistry research due to its unique structural features and potential applications in the development of pharmaceuticals and biologically active compounds.
Uses
Used in Pharmaceutical Synthesis:
(+/-)-cis-(4-hydroxymethyl)cyclopent-2-en-1-ylamine is used as a building block for the synthesis of various pharmaceuticals and biologically active compounds. Its unique structure allows for the creation of a wide range of molecules with potential therapeutic properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (+/-)-cis-(4-hydroxymethyl)cyclopent-2-en-1-ylamine is used as a valuable and versatile compound for the development of novel drug candidates. Its structural features make it an interesting target for research, with studies showing its potential in the development of new drug therapies for various diseases.
Used in Organic Synthesis:
(+/-)-cis-(4-hydroxymethyl)cyclopent-2-en-1-ylamine is also utilized in organic synthesis, where it serves as a key intermediate for the production of complex organic molecules. Its reactivity and functional groups make it a useful component in the synthesis of a variety of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 122624-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,6,2 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122624-72:
(8*1)+(7*2)+(6*2)+(5*6)+(4*2)+(3*4)+(2*7)+(1*2)=100
100 % 10 = 0
So 122624-72-0 is a valid CAS Registry Number.
122624-72-0Relevant articles and documents
Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction
Shinde, Madhuri V.,Ople, Rohini S.,Sangtani, Ekta,Gonnade, Rajesh,Reddy, D. Srinivasa
, p. 1060 - 1067 (2015)
A novel and convenient method utilizing the Aubé reaction to access a new class of compounds that are similar to carbocyclic nucleosides is reported. The azido alcohol derived from Vince lactam undergoes the Aubé reaction with various cyclic ketones to gi
Deamination of 9-(hydroxymethylated cycloalkyl)-9H-adenines (carbocyclic adenine nucleosides) by adenosine deaminase: Effect of high-pressure upon deamination rate and enantioselectivity
Katagiri, Nobuya,Ito, Yumiko,Shiraishi, Takuya,Maruyama, Tokumi,Sato, Yoshiko,Kaneko, Chikara
, p. 631 - 647 (2007/10/03)
The deamination of eight kinds of racemic carbocyclic adenine nucleosides by adenosine deaminase under high-pressure (400 MPa) was examined and the result was compared with that obtained from the reaction under atmospheric pressure. The deamination of all
Synthesis of carbocyclic nucleosides from 2-azabicyclo[2.2.1]hept-5-en-3-ones: Sodium borohydride-mediated carbon-nitrogen bond cleavage of five- and six-membered lactams
Katagiri,Muto,Nomura,Higashikawa,Kaneko
, p. 1112 - 1122 (2007/10/02)
Various carbocyclic ribofuranosyl nucleosides were stereoselectively synthesized through a small number of steps from 2-azabicyclo[2.2.1]hept-5-en-3-ones by the use of sodium borohydride-mediated C-N bond cleavage as a key step. Ready availability of a no
