911313-90-1 Usage
Description
(S)-3-(Benzyloxy)pyrrolidine, with the molecular formula C11H15NO, is a pyrrolidine derivative that exists as a white to off-white solid substance. It has a molecular weight of 177.24 g/mol and is characterized by the presence of a benzyloxy group attached to the pyrrolidine ring. (S)-3-(BENZYLOXY)PYRROLIDINE is significant in organic chemistry and drug discovery due to its role as a building block in the synthesis of pharmaceuticals and agrochemicals. The benzyloxy group provides a reactive site for further chemical reactions, making it a valuable intermediate in the creation of various compounds. Moreover, (S)-3-(Benzyloxy)pyrrolidine may also possess biological activity, which is currently being investigated for potential pharmacological applications.
Uses
Used in Pharmaceutical Industry:
(S)-3-(Benzyloxy)pyrrolidine is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure and the presence of the benzyloxy group make it a versatile intermediate in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-3-(Benzyloxy)pyrrolidine is utilized as a key component in the production of various agrochemicals. Its chemical properties allow for the creation of compounds that can be used in the development of pesticides, herbicides, and other agricultural products.
Used in Organic Synthesis:
(S)-3-(Benzyloxy)pyrrolidine is employed as a valuable intermediate in organic synthesis. The benzyloxy group attached to the pyrrolidine ring provides a reactive site for further chemical reactions, enabling the synthesis of a wide range of compounds with diverse applications.
Used in Drug Discovery:
(S)-3-(Benzyloxy)pyrrolidine is studied for its potential biological activity and pharmacological applications. Researchers are exploring its properties to identify possible uses in the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 911313-90-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,3,1 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 911313-90:
(8*9)+(7*1)+(6*1)+(5*3)+(4*1)+(3*3)+(2*9)+(1*0)=131
131 % 10 = 1
So 911313-90-1 is a valid CAS Registry Number.
911313-90-1Relevant articles and documents
Synthesis of chiral five-, six-, and seven-membered heterocycles from (S)-3-hydroxy-γ-butyrolactone
Yang, Hao,Goyal, Navneet,Ella-Menye, Jean Rene,Williams, Kristopher,Wang, Guijun
, p. 561 - 568 (2012/05/05)
Chiral small molecules such as amino alcohols and their heterocyclic derivatives are useful building blocks for asymmetric synthesis and the preparation of biologically active compounds. Using a common starting material derived from carbohydrate, the (S)-3-hydroxy - butyrolactone, we have synthesized several five-, six-, and seven-membered nitrogen-containing chiral heterocycles. These include (S)-3-benzyloxypyrrolidine, a protected 6-substituted morpholin-3-one and its homologous 1,4-oxazepan-3-one, and 6-trityloxymethyl tetrahydro-1,3-oxazine-2-thiones. These chiral small heterocycles were synthesized from the lactone via efficient cyclization reactions. Their syntheses and characterization are reported here. Georg Thieme Verlag Stuttgart - New York.
3-[2-(Pyrrolidin-1-yl)ethyl]indoles and 3-[3-(Piperidin-1- yl)propyl]indoles: Agonists for the h5-HT(1D) receptor with high selectivity over the h5-HT(1B) subtype
Castro,Street,Guiblin,Jelley,Russell,Sternfeld,Beer,Stanton,Matassa
, p. 3497 - 3500 (2007/10/03)
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