Pyrrolidines

Organic heterocyclic compounds that consist of a five-membered ring with four carbon atoms and one nitrogen atom that form a cyclic secondary amine.

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496 – 510 of 6,160 results

496

Ambeed AMBEED

5000868494 S-PYRROLIDINE-3-CARBONITRI 1GR

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497

eMolecules 887922-93-2 | 3-(Pyrrolidin-1-ylmethyl)benzoic acid hydrochloride | Combi-Blocks | MFCD08690301 | 241.720 | C12H16ClNO2 | 97.000 | Cl.OC(=O)c1cccc(CN2CCCC2)c1 | 1g | 290705235

3-(Pyrrolidin-1-ylmethyl)benzoic acid hydrochloride | Combi-Blocks | 887922-93-2 | MFCD08690301 | 241.720 | C12H16ClNO2 | 97.000 | Cl.OC(=O)c1cccc(CN2CCCC2)c1 | 1g | 290705235

Pricing & Availability

498

eMolecules 7661-32-7 | 1-(4-Bromophenyl)pyrrolidin-2-one | Combi-Blocks | MFCD00138502 | 240.100 | C10H10BrNO | 98.000 | Brc1ccc(cc1)N1CCCC1=O | 1g | 117543619

1-(4-Bromophenyl)pyrrolidin-2-one | Combi-Blocks | 7661-32-7 | MFCD00138502 | 240.100 | C10H10BrNO | 98.000 | Brc1ccc(cc1)N1CCCC1=O | 1g | 117543619

Pricing & Availability

499

eMolecules 1257648-75-1 | 2-(Pyrrolidin-1-yl)pyridine-3-boronic acid | Combi-Blocks | MFCD11867875 | 192.030 | C9H13BN2O2 | 95.000 | OB(O)c1cccnc1N1CCCC1 | 5g | 205382486

2-(Pyrrolidin-1-yl)pyridine-3-boronic acid | Combi-Blocks | 1257648-75-1 | MFCD11867875 | 192.030 | C9H13BN2O2 | 95.000 | OB(O)c1cccnc1N1CCCC1 | 5g | 205382486

Pricing & Availability

500

eMolecules 887922-93-2 | 3-(Pyrrolidin-1-ylmethyl)benzoic acid hydrochloride | Combi-Blocks | MFCD08690301 | 241.720 | C12H16ClNO2 | 97.000 | Cl.OC(=O)c1cccc(CN2CCCC2)c1 | 250mg | 359296751

3-(Pyrrolidin-1-ylmethyl)benzoic acid hydrochloride | Combi-Blocks | 887922-93-2 | MFCD08690301 | 241.720 | C12H16ClNO2 | 97.000 | Cl.OC(=O)c1cccc(CN2CCCC2)c1 | 250mg | 359296751

Pricing & Availability

501

eMolecules 51535-00-3 | Methyl 1-benzyl-5-oxo-3-pyrrolidinecarboxylate | Combi-Blocks | MFCD00003196 | 233.267 | C13H15NO3 | 98.000 | COC(=O)C1CN(Cc2ccccc2)C(=O)C1 | 1g | 232338086

Methyl 1-benzyl-5-oxo-3-pyrrolidinecarboxylate | Combi-Blocks | 51535-00-3 | MFCD00003196 | 233.267 | C13H15NO3 | 98.000 | COC(=O)C1CN(Cc2ccccc2)C(=O)C1 | 1g | 232338086

Pricing & Availability

502

eMolecules 886500-65-8 | 2-Chloro-4-(pyrrolidino)benzaldehyde | Combi-Blocks | MFCD06740077 | 209.670 | C11H12ClNO | 98.000 | Clc1cc(ccc1C=O)N1CCCC1 | 1g | 205393334

2-Chloro-4-(pyrrolidino)benzaldehyde | Combi-Blocks | 886500-65-8 | MFCD06740077 | 209.670 | C11H12ClNO | 98.000 | Clc1cc(ccc1C=O)N1CCCC1 | 1g | 205393334

Pricing & Availability

503

eMolecules 886500-65-8 | 2-Chloro-4-(pyrrolidino)benzaldehyde | Combi-Blocks | MFCD06740077 | 209.670 | C11H12ClNO | 98.000 | Clc1cc(ccc1C=O)N1CCCC1 | 5g | 205393335

2-Chloro-4-(pyrrolidino)benzaldehyde | Combi-Blocks | 886500-65-8 | MFCD06740077 | 209.670 | C11H12ClNO | 98.000 | Clc1cc(ccc1C=O)N1CCCC1 | 5g | 205393335

Pricing & Availability

504

Sigma Aldrich Fine Chemicals Biosciences 1 Methyl 2 pyrrolidinone b

N-Methyl-2-pyrrolidinone (N-methylpyrrolidone NMP) is a polar cyclic organic solvent. A study on the impact of NMP on Saccharomyces cerevisiae revealed that it induced aneuploidy. Characteristic properties of NMP include low viscosity excellent dissolving power and enhanced demulsifying property. It is a better alternative to phenol in selectively treating lube feedstock. The behavior of fullerene-C60 in NMP SOLUTIONon has been examined based on electronic absorption and photoluminescence spectral data. A SOLUTIONon of sodium borohydride (NaBH4) in NMP showed increased reactivity towards debromination of alkyl bromide. The enhanced selectivity of NMP-ethylene glycol solvent mixture for aromatic hydrocarbon extraction has been analyzed by gas chromatography.

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505

Sigma Aldrich Fine Chemicals Biosciences Z VAD FMK solid2MG

Z-VAD-FMK inhibits yeast and mammalian peptide N-glycanase (PNGase). It induces apoptosis. Z-VAD-FMK might be associated with endoplasmic reticulum (ER) stress.