Home Amines 79286-79-6
79286-79-6,MFCD00059018
Catalog No.:AA003IVC
79286-79-6 | pyrrolidin-3-amine
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1g
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$15.00   $10.00
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5g
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$35.00   $24.00
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25g
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100g
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  • Technical Information
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Technical Information
Catalog Number:
AA003IVC
Chemical Name:
pyrrolidin-3-amine
CAS Number:
79286-79-6
Molecular Formula:
C4H10N2
Molecular Weight:
86.1356
MDL Number:
MFCD00059018
IUPAC Name:
pyrrolidin-3-amine
InChI:
InChI=1S/C4H10N2/c5-4-1-2-6-3-4/h4,6H,1-3,5H2
InChI Key:
NGXSWUFDCSEIOO-UHFFFAOYSA-N
SMILES:
NC1CNCC1
Properties
Computed Properties
 
Complexity:
44.8  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
86.084g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
86.138g/mol
Monoisotopic Mass:
86.084g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
38A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.9  

Synonyms
 
3-Aminopyrrolidine 
79286-79-6 
3-Pyrrolidinamine # 
Pyrrolidin-3-ylamine 
PubChem9196 
pyrrolidine-3-ylamine 
PubChem20096 
ACMC-209bew 
AC1L4UPV 
ACMC-1CC1G 
(3RS)-3-aminopyrrolidine 
AC1Q53IP 
pyrrolidin-3-amine 
AC1Q53IQ 
3-Pyrrolidinamine, AldrichCPR 
ACMC-2099s2 
3-aminopyrrolidineDihydrochloride 
CTK2H7045 
DTXSID70276538 
ALBB-005927 
ANW-37278 
MFCD00059018 
SBB027337 
3-Pyrrolidinamine 
STK503626 
AKOS009159382 
AN-1681 
CS-W004336 
MCULE-2237528072 
TRA0065984 
TRA0077042 
TRA0084823 
VP60165 
VP60188 
NGXSWUFDCSEIOO-UHFFFAOYSA-N 
KS-000016Z2 
AK-80471 
R826 
SC-18208 
DB-006351 
TC-030714 
4CH-018085 
FT-0600346 
FT-0602175 
FT-0604729 
(3S)-(-)-Aminopyrrolidine 
ST24025739 
A80215 
Y-9399 
3-Aminopyrrolidine Dihydrochloride Dihydrochloride 
A839637 
I11-0008 
I11-0035 
I11-0038 
I11-0066 
(R)-pyrrolidin-3-amine 
3aminopyrrolidine 
aminopyrrolidine 
(S)-pyrrolidin-3-amine 
(R)-3-Aminopyrrolidine 
(S)-3-Aminopyrrolidine 
pyrrolidin-3-amine dihydrochloride 
(3R)-(+)-3-Aminopyrrolidine 
(3S)-(-)-3-Aminopyrrolidine 
C4H10N2 
3-Aminopyrrolidine dihydrochloride 
CID164401 
3-amino pyrrolidine 
116183-82-5 
A1104 
A1883 
128345-57-3 
103831-11-4 
3-amino-pyrrolidine 
pyrrolidine-3-amine 
Literature

Title: Structural insights from binding poses of CCR2 and CCR5 with clinically important antagonists: a combined in silico study.

Journal: PloS one 20120101

Title: 3D-QSAR studies on CCR2B receptor antagonists: Insight into the structural requirements of (R)-3-aminopyrrolidine series of molecules based on CoMFA/CoMSIA models.

Journal: Journal of pharmacy & bioallied sciences 20120101

Title: Metabolic profiling of the protozoan parasite Entamoeba invadens revealed activation of unpredicted pathway during encystation.

Journal: PloS one 20120101

Title: Semi-quantitative analyses of metabolic systems of human colon cancer metastatic xenografts in livers of superimmunodeficient NOG mice.

Journal: Analytical and bioanalytical chemistry 20110601

Title: Exploration of (S)-3-aminopyrrolidine as a potentially interesting scaffold for discovery of novel Abl and PI3K dual inhibitors.

Journal: European journal of medicinal chemistry 20110401

Title: Design of selective, ATP-competitive inhibitors of Akt.

Journal: Journal of medicinal chemistry 20100624

Title: Synthesis and biological evaluation of 3-aminopyrrolidine derivatives as CC chemokine receptor 2 antagonists.

Journal: Bioorganic & medicinal chemistry letters 20100401

Title: Design of novel aminopyrrolidine factor Xa inhibitors from a screening hit.

Journal: European journal of medicinal chemistry 20090701

Title: Elucidation of binding sites of dual antagonists in the human chemokine receptors CCR2 and CCR5.

Journal: Molecular pharmacology 20090601

Title: Synthesis and antimalarial activity of new amino analogues of amodiaquine.

Journal: Medicinal chemistry (Shariqah (United Arab Emirates)) 20080901

Title: Dual-targeting properties of the 3-aminopyrrolidyl quinolones, DC-159a and sitafloxacin, against DNA gyrase and topoisomerase IV: contribution to reducing in vitro emergence of quinolone-resistant Streptococcus pneumoniae.

Journal: The Journal of antimicrobial chemotherapy 20080701

Title: Potent antagonists of the CCR2b receptor. Part 3: SAR of the (R)-3-aminopyrrolidine series.

Journal: Bioorganic & medicinal chemistry letters 20080315

Title: New insight for fluoroquinophenoxazine derivatives as possibly new potent topoisomerase I inhibitor.

Journal: Bioorganic & medicinal chemistry letters 20080215

Title: 3-Aminopyrrolidines from alpha-aminoacids: total synthesis of (+)-nemonapride from D-alanine.

Journal: The Journal of organic chemistry 20080201

Title: Palladium-mediated N-arylation of heterocyclic diamines: insights into the origin of an unusual chemoselectivity.

Journal: The Journal of organic chemistry 20070316

Title: Enantioselective conjugate addition of a lithium ester enolate catalyzed by chiral lithium amides.

Journal: Organic letters 20061207

Title: Identification of substituted 4-aminopiperidines and 3-aminopyrrolidines as potent MCH-R1 antagonists for the treatment of obesity.

Journal: Bioorganic & medicinal chemistry letters 20061015

Title: Bis(aminopyrrolidine)-derived ureas (APUs) as potent MCH1 receptor antagonists.

Journal: Bioorganic & medicinal chemistry letters 20050215

Title: Palladium-mediated arylation of 3-aminopiperidines and 3-aminopyrrolidines.

Journal: The Journal of organic chemistry 20041210

Title: Design and synthesis of novel biologically active thrombin receptor non-peptide mimetics based on the pharmacophoric cluster Phe/Arg/NH2 of the Ser42-Phe-Leu-Leu-Arg46 motif sequence: platelet aggregation and relaxant activities.

Journal: Journal of medicinal chemistry 20040617

Title: A NMR and theoretical study of the aggregates between alkyllithium and chiral lithium amides: control of the topology through a single asymmetric center.

Journal: Journal of the American Chemical Society 20021225

Title: Synthesis and structure-activity relationships of novel 7-substituted 1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acids as antitumor agents. Part 1.

Journal: Journal of medicinal chemistry 20021205

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