CAS 101469-92-5
:1-Pyrrolidinecarboxylic acid, 3-hydroxy-, 1,1-dimethylethyl ester, (3S)-
Description:
1-Pyrrolidinecarboxylic acid, 3-hydroxy-, 1,1-dimethylethyl ester, (3S)-, commonly referred to by its CAS number 101469-92-5, is an organic compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. This compound features a carboxylic acid functional group and a hydroxy group, contributing to its potential as a chiral building block in organic synthesis. The presence of the tert-butyl ester group enhances its lipophilicity, making it more soluble in organic solvents. As a chiral molecule, it exhibits stereoisomerism, with the (3S) designation indicating the specific spatial arrangement of its atoms. This compound may be of interest in pharmaceutical applications due to its structural features that can influence biological activity. Additionally, its synthesis and reactivity can be explored in various chemical reactions, including esterification and hydrolysis. Overall, 1-Pyrrolidinecarboxylic acid, 3-hydroxy-, 1,1-dimethylethyl ester, (3S)- is a versatile compound with potential applications in medicinal chemistry and organic synthesis.
Formula:C9H17NO3
InChI:InChI=1S/C9H17NO3/c1-9(2,3)13-8(12)10-5-4-7(11)6-10/h7,11H,4-6H2,1-3H3/t7-/m0/s1
InChI key:InChIKey=APCBTRDHCDOPNY-ZETCQYMHSA-N
SMILES:C(OC(C)(C)C)(=O)N1CC[C@H](O)C1
Synonyms:- (+)-N-Boc-3-hydroxypyrrolidine
- (3S)-1-Boc-3-hydroxypyrrolidine
- (3S)-1-Boc-3-pyrrolidinol
- (3S)-1-tert-Butoxycarbonyl-3-hydroxypyrrolidine
- (3S)-1-tert-Butoxycarbonyl-3-pyrrolidinol
- (3S)-3-Hydroxypyrrolidine-1-carboxylic acid tert-butyl ester
- (3S)-Hydroxypyrrolidine-1-carboxylic acid tert-butyl ester
- (3S)-N-tert-Butoxycarbonylpyrrolidin-3-ol
- (S)-(+)-N-(tert-Butoxycarbonyl)-3-hydroxypyrrolidine
- (S)-(+)-N-(tert-Butoxycarbonyl)-3-pyrrolidinol
- (S)-(+)-N-Boc-3-hydroxypyrrolidine
- (S)-1-(tert-Butoxycarbonyl)-3-pyrrolidinol
- (S)-1-BOC-3-Pyrrolidinol
- (S)-1-Boc-3-Hydroxylpyrrolidine
- (S)-1-Boc-3-Hydroxypyrrolidine
- (S)-1-N-Boc-3-Hydroxypyrrolidine
- (S)-1-N-Boc-3-pyrrolidinol
- (S)-1-tert-Butoxycarbonyl-3-hydroxypyrrolidine
- (S)-3-Hydroxy-1-(tert-butoxycarbonyl)pyrrolidine
- (S)-3-Hydroxy-1-Boc-pyrrolidine
- (S)-3-Hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester
- (S)-3-Hydroxypyrrolidine-1-carboxylic acid tert-butyl ester
- (S)-N-(t-Butyloxycarbonyl)-3-hydroxypyrrolidine
- (S)-N-Boc-3-pyrrolidinol
- (S)-Tert-Butyl 3-Hydroxypyrrolidine-1-Carboxylate
- 1,1-Dimethylethyl (3S)-3-hydroxy-1-pyrrolidinecarboxylate
- 1,1-Dimethylethyl (3S)-3-hydroxypyrrolidine-1-carboxylate
- 1-Pyrrolidinecarboxylic Acid, 3-Hydroxy-, 1,1-Dimethylethyl Ester, (3S)-
- 1-Pyrrolidinecarboxylic acid, 3-hydroxy-, 1,1-dimethylethyl ester, (S)-
- 2-Methyl-2-Propanyl (3S)-3-Hydroxy-1-Pyrrolidinecarboxylate
- N-(tert-Butoxycarbonyl)-(S)-(+)-3-pyrrolidinol
- N-Boc-(S)-3-hydroxypyrrolidine
- N-[(tert-Butoxy)carbonyl]-(S)-3-hydroxypyrrolidine
- S-1-N-Boc-3-Hydroxy Pyrrolidine
- tert-Butyl (1S)-3-hydroxypyrrolidine-1-carboxylate
- tert-Butyl (S)-3-hydroxypyrrolidine-1-carboxylate
- tert-Butyl-(3S)-3-hydroxypyrrolidin-1-carboxylate
- tert-butyl (3R)-3-hydroxypyrrolidine-1-carboxylate
- See more synonyms
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Found 7 products.
(S)-1-(Tert-Butoxycarbonyl)-3-Hydroxypyrrolidine
CAS:Formula:C9H17NO3Purity:97%Color and Shape:SolidMolecular weight:187.2362(S)-1-(tert-Butoxycarbonyl)-3-pyrrolidinol
CAS:Formula:C9H17NO3Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:187.24(3S)-3-Hydroxypyrrolidine, N-BOC protected
CAS:<p>(3S)-3-Hydroxypyrrolidine, N-BOC protected</p>Formula:C9H17NO3Purity:97%Color and Shape: pale yellow solidMolecular weight:187.24g/mol(S)-1-N-Boc-3-Hydroxy-pyrrolidine
CAS:Formula:C9H17NO3Purity:97%Color and Shape:Solid, Chunks or Crystalline PowderMolecular weight:187.239(S)-N-Boc-3-hydroxypyrrolidine
CAS:<p>(S)-N-Boc-3-hydroxypyrrolidine is a selective, non-competitive reuptake inhibitor of serotonin. It has been shown to be a penetrant and can cross the blood-brain barrier. (S)-N-Boc-3-hydroxypyrrolidine has also been shown to inhibit DNA methyltransferases and may have antidepressant effects. This drug is thought to act as a substrate for catecholamine neurotransmitter synthesis and may be useful in the treatment of symptoms associated with depression.</p>Formula:C9H17NO3Purity:Min. 95%Color and Shape:White To Yellow SolidMolecular weight:187.24 g/mol






