91790-91-9

Basic information

• Product Name: (S)-4-(2-PYRROLIDINYLMETHYL)MORPHOLINE
• Synonyms: (S)-4-(2-PYRROLIDINYLMETHYL)MORPHOLINE;OTAVA-BB 7020690605;(2S)-2-[(Morpholin-4-yl)methyl]pyrrolidine;(S)-2-((Morpholin-4-yl)methyl)pyrrolidine;(S)-2-Morpholinomethylpyrrolidine;4-[(2S)-Pyrrolidin-2-ylmethyl]morpholine;4-[(2S)-PyrrolidinylMethyl]Morpholine;(S)-4-(2-PyrrolidinylMethyl)Morpholine 2HCl
• CAS NO: 91790-91-9
• Molecular Formula: C9H18N2O
• Molecular Weight: 170.25
• Mol File: 91790-91-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 255℃
• Flash Point: 108℃
• Appearance: /
• Density: 1.019
• CAS DataBase Reference: (S)-4-(2-PYRROLIDINYLMETHYL)MORPHOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-(2-PYRROLIDINYLMETHYL)MORPHOLINE(91790-91-9)
• EPA Substance Registry System: (S)-4-(2-PYRROLIDINYLMETHYL)MORPHOLINE(91790-91-9)

Safety Data

• Hazardous Substances Data: 91790-91-9(Hazardous Substances Data)

Usage

General Description

"(S)-4-(2-Pyrrolidinylmethyl)morpholine" is a chemical compound with the molecular formula C12H22N2O. It is an organic compound that contains a morpholine ring and a pyrrolidine ring, and is classified as a morpholine derivative. (S)-4-(2-PYRROLIDINYLMETHYL)MORPHOLINE is a chiral molecule, meaning it has two enantiomers, the (S)- and (R)- forms. It has been found to have various applications in the pharmaceutical and chemical industries, including as a chiral auxiliary in the synthesis of biologically active compounds, and as a building block for the synthesis of potential therapeutic agents. Additionally, the (S)-4-(2-Pyrrolidinylmethyl)morpholine has also been investigated for its potential use as a ligand in the coordination chemistry field.

Upstream product

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• 1148-11-4 N-Benzyloxycarbonyl-L-proline 
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• 1013941-83-7 2-(R,S)-5-(S)-<3.3.0>-1-aza-2-thia-3-oxabicyclooctane-2-oxide 
• 23356-96-9 (S)-1-Pyrrolidin-2-yl-methanol 
• 52682-03-8 (S)(-)-N,O-bis(p-toluenesulphonyl)-2-hydroxymethyl pyrrolidine 
• 114671-25-9 (S)-N-(p-toluenesulphonyl)-2-(morpholinomethyl) pyrrolidine 
• 73094-26-5 morpholino(pyrrolidin-2-yl)methanone 
• 110-91-8 morpholine 
• 132635-95-1 5-(S)-<3.3.0>-1-aza-2-thia-3-oxabicyclooctane-2,2-dioxide 

Relevant articles and documents

NOVEL BETULINIC SUBSTITUTED AMIDE DERIVATIVES AS HIV INHIBITORS

The present invention relates to novel betulinic substituted amide compounds of formula (I); and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6, R7, R8, X, Y, Z1, Z2, Z3 and are Formula (II) as defined herein. The invention novel betulinic substituted amide derivatives, related compounds, and pharmaceutical compositions useful for the therapeutic treatment of viral diseases and particularly HIV mediated diseases.

Thiophene derivatives useful as anticancer agents

The invention relates to compounds of the formula 1 or a pharmaceutically acceptable salt and to pharmaceutically acceptable salts and hydrates thereof, wherein X, Y, R1, R2 and R11 are as defined herein. The invention also relates to pharmaceutical compositions containing the compounds of formula 1 and to methods of treating hyperproliferative disorders in a mammal by administering the compounds of formula 1.

The direct synthesis of the cyclic sulphamidate of (S)-prolinol: Simultaneous N-protection and activation towards nucleophilic displacement of oxygen

The preparation of the cyclic sulphamidate of (S)-prolinol has been achieved by reaction with sulphuryl chloride at low temperature. This material has been shown to be susceptible to acid catalysed nucleophilic attack to furnish 2-(N,N-dialkylamino)methyl- and 2-(methoxymethyl)pyrrolidines after hydrolysis of the intermediate sulphamic acid derivatives.