1279200-14-4 Usage
General Description
(2R,4S)-benzyl 4-amino-2-(hydroxymethyl)pyrrolidine-1-carboxylate is a chemical compound with the molecular formula C15H20N2O3. It is a derivative of pyrrolidine, containing a benzyl and an amino group, as well as a hydroxymethyl substituent on the 2-position. (2R,4S)-benzyl 4-amino-2-(hydroxymethyl)pyrrolidine-1-carboxylate has potential applications in medicinal chemistry, particularly in the development of drugs targeting the pyrrolidine receptor. Its stereochemistry, with 2R and 4S configurations, is important for its biological activity and interactions with other molecules. This chemical may also be of interest in organic synthesis and as a building block for more complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 1279200-14-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,9,2,0 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1279200-14:
(9*1)+(8*2)+(7*7)+(6*9)+(5*2)+(4*0)+(3*0)+(2*1)+(1*4)=144
144 % 10 = 4
So 1279200-14-4 is a valid CAS Registry Number.
1279200-14-4Relevant articles and documents
Preparation method for (1S,4S)-2,5-diazabicyclo[2.2.1]heptane or (1S,4S)-2,5-diazabicyclo [2.2.1]octane derivative
-
Paragraph 0070; 0076; 0077, (2017/06/02)
The invention discloses a preparation method for a (1S,4S)-2,5-diazabicyclo[2.2.1]heptane or (1S,4S)-2,5-diazabicyclo [2.2.1]octane derivative. The method comprises the following steps: subjecting a hydroxyl group of five-component or six-component N-heterocycle to sulfonylation by using a sulfonylation reagent; then subjecting sulfonate to a substitution reaction of SN2 by using an azide; simultaneously reducing an azido group and an ester group by using a reduction reaction; and finally, carrying out ring closure so as to obtain the derivative. The synthesis route of the preparation method has higher selectivity compared with the prior art; reaction steps are reduced; cost for raw materials and time cost are saved; product yield is substantially higher than product yield in the prior art; and the preparation method can easily realize purification and enlarged production and reduce discharging of waste.
