Home>>(1R,3S)-3-Aminomethyl-cyclopentanol

(1R,3S)-3-Aminomethyl-cyclopentanol Sale

(Synonyms: (1R,3S)-3-(氨基甲基)环戊烷-1-醇) 目录号 : GC41687

(1R,3S)-3-Aminomethyl-cyclopentanol is a synthetic intermediate useful for pharmaceutical synthesis.

(1R,3S)-3-Aminomethyl-cyclopentanol Chemical Structure

Cas No.:1110772-09-2

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50mg
¥1,165.00
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产品描述

(1R,3S)-3-Aminomethyl-cyclopentanol is a synthetic intermediate useful for pharmaceutical synthesis.

Chemical Properties

Cas No. 1110772-09-2 SDF
别名 (1R,3S)-3-(氨基甲基)环戊烷-1-醇
Canonical SMILES O[C@H]1C[C@@H](CN)CC1
分子式 C6H13NO 分子量 115.2
溶解度 Soluble in DMSO 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 8.6806 mL 43.4028 mL 86.8056 mL
5 mM 1.7361 mL 8.6806 mL 17.3611 mL
10 mM 0.8681 mL 4.3403 mL 8.6806 mL
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Research Update

[(1R,3S)-3-(1,3-Dithian-2-yl)-2,2-dimethyl-cyclo-prop-yl]diphenyl-methanol

Acta Crystallogr Sect E Struct Rep Online 2009 May 7;65(Pt 6):o1230.PMID:21583098DOI:10.1107/S1600536809016079.

In the title compound, C(22)H(26)OS(2), prepared from (-)-1R-cis-caronaldehyde, the 1,3-dithiane ring adopts a chair conformation. An intra-molecular O-H⋯S hydrogen bond influences the mol-ecular conformation. In the crystal, weak inter-molecular C-H⋯S and C-H⋯O hydrogen bonds link the mol-ecules into chains propagating along [010].

(1R,3S,4R,4aS,7R,7aS,10R,12aR)-3-Azido-4,7,10-trimethyl-1,10-epidioxy-per-hydropyrano[4,3-j][1,2]benzodiox-epine

Acta Crystallogr Sect E Struct Rep Online 2010 Jun 26;66(Pt 7):o1839.PMID:21588040DOI:10.1107/S1600536810024566.

In the title compound, C(15)H(23)N(3)O(4), the six-membered pyran, cyclo-hexane and trioxane rings adopt chair, chair and boat conformations, respectively, while the seven-membered rings adopt distorted boat and very distorted chair conformations. In the crystal, adjacent mol-ecules are connected by weak C-H⋯N and C-H⋯O inter-actions.

(1R,3S,8R)-3,7,7,10-Tetra-methyl-tri-cyclo-[6.4.0.0(1,3)]dodec-9-en-11-one

Acta Crystallogr Sect E Struct Rep Online 2013 Dec 21;70(Pt 1):o81-2.PMID:24527013DOI:10.1107/S1600536813034041.

The absolute configuration of the title compound, C16H24O, has been deduced from the chemical pathway. The six-membered ring has a roughly half-chair conformation with the quaternary C atom as the flap. The seven-membered ring displays a chair conformation. In the crystal, there is a weak C-H⋯O hydrogen bond between the methyl-ene group of the cyclo-propane ring and the carbonyl group of a screw-axis-related mol-ecule, which builds up a zigzag-like chain along the b-axis direction.

(1R,3S)-3-Hydroxy-meth-yl-N-isopropyl-2,2-dimethyl-cyclo-propane-carboxamide

Acta Crystallogr Sect E Struct Rep Online 2009 Dec 12;66(Pt 1):o118.PMID:21580007DOI:10.1107/S1600536809051538.

The asymmetric unit of the title compound, C(10)H(19)NO(2), prepared from (-)-1R-cis-caronaldehyde, contains two independent mol-ecules. In the crystal structure, inter-molecular O-H⋯O and O-H⋯N hydrogen bonds form an extensive three-dimensional hydrogen-bonding network.

[(1R,3S)-6,7-Dimeth-oxy-1-phenyl-1,2,3,4-tetra-hydro-isoquinolin-3-yl]methanol 2.33-hydrate

Acta Crystallogr Sect E Struct Rep Online 2011 Feb 23;67(Pt 3):o700.PMID:21522445DOI:10.1107/S1600536811006052.

The title compound, C(18)H(21)NO(3)·2.33H(2)O, is the fourth reported member in a series of (1R,3S)-6,7-dimeth-oxy-1-phenyl-1,2,3,4-tetra-hydro-isoquinoline derivatives used in catalysis as ligands (or their precursors). The N-heterocycle in the structure adopts a half-chair conformation. The dihedral angle between the benzene rings is 77.29 (13)°. There are three ill-resolved water molecules of crystallization in the structure (one of them rotationally disordered about a threefold axis) involved in short contacts probably due to hydrogen bonding.