114214-73-2 Usage
Uses
Used in Pharmaceutical Industry:
1-Boc-3-(aminomethyl)-3-hydroxypyrrolidine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the creation of complex molecular structures. Its protected amino alcohol nature allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Boc-3-(aminomethyl)-3-hydroxypyrrolidine is utilized as a building block for the preparation of bioactive molecules that can be employed in the development of pesticides, herbicides, and other crop protection agents. Its versatility in synthesis contributes to the creation of effective and targeted agrochemicals.
Used in Medicinal Chemistry Research:
1-Boc-3-(aminomethyl)-3-hydroxypyrrolidine is used as a research tool in medicinal chemistry to explore its potential in the development of new therapeutic agents. Its unique structure allows scientists to investigate its interactions with biological targets and its potential to treat various diseases.
Used in Organic Synthesis:
As a versatile building block, 1-Boc-3-(aminomethyl)-3-hydroxypyrrolidine is used in organic synthesis for the preparation of a wide range of compounds. Its protected amino alcohol functionality makes it an ideal candidate for the synthesis of complex organic molecules with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 114214-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,2,1 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114214-73:
(8*1)+(7*1)+(6*4)+(5*2)+(4*1)+(3*4)+(2*7)+(1*3)=82
82 % 10 = 2
So 114214-73-2 is a valid CAS Registry Number.
114214-73-2Relevant academic research and scientific papers
Geoghegan, Kimberly,Bode, Jeffrey W.
, p. 1934 - 1937 (2015)
The precise placement of C-substituents on bicyclic and spirocyclic N-heterocycles is readily achieved by the combination of aldehydes and new SnAP reagents. The substituted SnAP reagents are readily prepared from simple starting materials and couple with
Quinoline-3-carboxylic acid derivatives
-
, (2008/06/13)
Compounds of formula (I): STR1 (in which R1 is alkoxy, R is alkyl, haloalkyl, alkylamino, cycloalkyl or optionally substituted phenyl, X is chlorine or fluorine and Y is selected from certain specific heterocycles) have excellent antibacterial activity. They may be prepared by introducing the group represented by Y into the corresponding compound in which Y is replaced by a halogen atom.
