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23356-96-9

23356-96-9 | (S)-(+)-2-(Hydroxymethyl)Pyrrolidine

CAS No: 23356-96-9 Catalog No: AG0032FY MDL No:MFCD00005255

Product Description

Catalog Number:
AG0032FY
Chemical Name:
(S)-(+)-2-(Hydroxymethyl)Pyrrolidine
CAS Number:
23356-96-9
Molecular Formula:
C5H11NO
Molecular Weight:
101.1469
MDL Number:
MFCD00005255
IUPAC Name:
[(2S)-pyrrolidin-2-yl]methanol
InChI:
InChI=1S/C5H11NO/c7-4-5-2-1-3-6-5/h5-7H,1-4H2/t5-/m0/s1
InChI Key:
HVVNJUAVDAZWCB-YFKPBYRVSA-N
SMILES:
OC[C@@H]1CCCN1
EC Number:
245-605-2

Properties

Complexity:
56  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
101.084g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
101.149g/mol
Monoisotopic Mass:
101.084g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
32.3A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.3  

Literature

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120-day comparative analysis of adhesion grade and quantity, mesh contraction, and tissue response to a novel omega-3 fatty acid bioabsorbable barrier macroporous mesh after intraperitoneal placement. Surgical innovation 20090301
(S)-2-(Iodo-meth-yl)-1-tosyl-pyrrolidine. Acta crystallographica. Section E, Structure reports online 20080101
Total synthesis of the putative structure of stemonidine: the definitive proof of misassignment. Organic letters 20070426
Synthesis, reaction, and recycle of fluorous palladium catalysts for an asymmetric allylic alkylation without using fluorous solvents. The Journal of organic chemistry 20050930
Development of chiral (S)-prolinol-derived ligands for palladium-catalyzed asymmetric allylic alkylation: effect of a siloxymethyl group on the pyrrolidine backbone. The Journal of organic chemistry 20041001
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