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3040-44-6

3040-44-6 | 2-(Piperidin-1-yl)ethanol

CAS No: 3040-44-6 Catalog No: AG00300W MDL No:MFCD00006512

Product Description

Catalog Number:
AG00300W
Chemical Name:
2-(Piperidin-1-yl)ethanol
CAS Number:
3040-44-6
Molecular Formula:
C7H15NO
Molecular Weight:
129.2001
MDL Number:
MFCD00006512
IUPAC Name:
2-piperidin-1-ylethanol
InChI:
InChI=1S/C7H15NO/c9-7-6-8-4-2-1-3-5-8/h9H,1-7H2
InChI Key:
KZTWONRVIPPDKH-UHFFFAOYSA-N
SMILES:
OCCN1CCCCC1
EC Number:
221-244-6
UNII:
VR81F07RX5
NSC Number:
3460

Properties

Complexity:
69.3  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
129.115g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
129.203g/mol
Monoisotopic Mass:
129.115g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
23.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1  

Literature

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In vitro cytotoxicity of benzopyranone derivatives with basic side chain against human lung cell lines. Anticancer research 20101101
The enhancing effect of ion-pairing on the skin permeation of glipizide. AAPS PharmSciTech 20090901
[Study on UV-Vis absorption spectra and fluorescence emission spectra of sixteen tetra-substituted metallophthalocyanine complexes]. Guang pu xue yu guang pu fen xi = Guang pu 20090501
Analogs of methyl-piperidinopyrazole (MPP): antiestrogens with estrogen receptor alpha selective activity. Bioorganic & medicinal chemistry letters 20090101
Synthesis of an optically pure synthetic intermediate of aloperine from a yeast-reductive product. Bioscience, biotechnology, and biochemistry 20050801
Selective estrogen receptor modulators with conformationally restricted side chains. Synthesis and structure-activity relationship of ERalpha-selective tetrahydroisoquinoline ligands. Journal of medicinal chemistry 20050127
Studies toward labeling cytisine with [11C]phosgene: rapid synthesis of a delta-lactam involving a new chemoselective lithiation-annulation method. The Journal of organic chemistry 20040528
Stereospecific rearrangements during the synthesis of pyrrolidines and related heterocycles from cyclizations of amino alcohols with vinyl Sulfones. The Journal of organic chemistry 20031128
Synthesis of sparteine-like chiral diamines and evaluation in the enantioselective lithiation-substitution of N-(tert-butoxycarbonyl)pyrrolidine. Organic & biomolecular chemistry 20031121
N-hydroxyethyl-piperidine and -pyrrolidine homoazasugars: preparation and evaluation of glycosidase inhibitory activity. Bioorganic & medicinal chemistry 20030731
Indolizino[1,2-b]quinolines derived from A-D rings of camptothecin: synthesis and DNA interaction. Journal of enzyme inhibition and medicinal chemistry 20030401
Formaldehyde-induced DNA cross-link of indolizino[1,2-b]quinolines derived from the A-D rings of camptothecin. Journal of medicinal chemistry 20021219
Triarylpyrazoles with basic side chains: development of pyrazole-based estrogen receptor antagonists. Bioorganic & medicinal chemistry 20010101

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