4-(Cbz-amino)-1-(methylsulfonyl)piperidine - CAS 402927-96-2

Catalog:	BB024432
Product Name:	4-(Cbz-amino)-1-(methylsulfonyl)piperidine
CAS:	402927-96-2
Synonyms:	N-(1-methylsulfonyl-4-piperidinyl)carbamic acid (phenylmethyl) ester; benzyl N-(1-methylsulfonylpiperidin-4-yl)carbamate

Technical Data

Patents

Computed Properties

IUPAC Name:	benzyl N-(1-methylsulfonylpiperidin-4-yl)carbamate
Description:	4-(Cbz-amino)-1-(methylsulfonyl)piperidine (CAS# 402927-96-2) is a useful research chemical.
Molecular Weight:	312.38
Molecular Formula:	C14H20N2O4S
Canonical SMILES:	CS(=O)(=O)N1CCC(CC1)NC(=O)OCC2=CC=CC=C2
InChI:	InChI=1S/C14H20N2O4S/c1-21(18,19)16-9-7-13(8-10-16)15-14(17)20-11-12-5-3-2-4-6-12/h2-6,13H,7-11H2,1H3,(H,15,17)
InChI Key:	PCUZCKVFKVUGIK-UHFFFAOYSA-N
LogP:	2.74640

Publication Number	Title	Priority Date
AU-2003215675-A1	Imidazo fused compounds	20020403
AU-2003215675-B2	Imidazo fused compounds	20020403
CA-2479644-A1	Imidazo fused compounds	20020403
US-2003232847-A1	Imidazo-substituted compounds as p38 kinase inhibitors	20020403
US-2005197352-A1	Imidazo-substituted compounds as p38 kinase inhibitors	20020403

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Related Functional Groups

Carbonyl Compounds

[89908-23-6]
2-Propenoic acid, 2-(3',3'-dimethyl-6-nitrospiro[2H-1-benzopyran-2,2'-[2H]indol]-1'(3'H)-yl)ethyl ester
[87-88-7]
Chloranilic acid
[959574-98-2]
(3-Phenyl-1H-pyrazol-1-yl)acetic acid
[1006443-01-1]
1-(5-Nitropyridin-2-yl)-1H-pyrazole-3-carboxylic acid
[70912-52-6]
1,3-Dioxane-4,6-dione,2,2-dimethyl-5-(2-pyrrolidinylidene)-
[59855-96-8]
2-(Methoxymethyl)thiazole-5-carboxylic Acid

Complexity:	432
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	312.1143783
Formal Charge:	0
Heavy Atom Count:	21
Hydrogen Bond Acceptor Count:	5
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	312.1143783
Rotatable Bond Count:	5
Topological Polar Surface Area:	84.1
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	1.3