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Merck
모든 사진(1)

주요 문서

446327

Sigma-Aldrich

N-Boc-L-prolinol

98%

동의어(들):

(S)-1-Boc-2-pyrrolidinemethanol

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About This Item

실험식(Hill 표기법):
C10H19NO3
CAS Number:
Molecular Weight:
201.26
Beilstein:
3542667
MDL number:
UNSPSC 코드:
12352209
PubChem Substance ID:
NACRES:
NA.22

분석

98%

양식

solid

광학 활성

[α]21/D −48°, c = 1.3 in chloroform

반응 적합성

reaction type: Boc solid-phase peptide synthesis

mp

62-64 °C (lit.)

응용 분야

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N1CCC[C@H]1CO

InChI

1S/C10H19NO3/c1-10(2,3)14-9(13)11-6-4-5-8(11)7-12/h8,12H,4-7H2,1-3H3/t8-/m0/s1

InChI key

BFFLLBPMZCIGRM-QMMMGPOBSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

Building block for novel nicotinic acetylcholine receptor ligands with cognition-enhancing properties. Used in the synthesis of chiral β-amino sulfides and β-amino thiols.
Used to synthesize anticoagulants.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Cran, G.A. et al.
Tetrahedron Asymmetry, 6, 1553-1553 (1995)
N H Lin et al.
Journal of medicinal chemistry, 40(3), 385-390 (1997-01-31)
2-Methyl-3-(2(S)-pyrrolidinylmethoxy)pyridine, ABT-089 (S-4), a member of the 3-pyridyl ether class of nicotinic acetylcholine receptor (nAChR) ligands, shows positive effects in rodent and primate models of cognitive enhancement and a rodent model of anxiolytic activity and possesses a reduced propensity to
Matthias Schulz et al.
Physical chemistry chemical physics : PCCP, 19(10), 6996-7008 (2017-02-28)
We suggest and explore a novel route towards organic photodetectors sensitive to the circular polarization state of light. For this, we insert fullerene-blended thin films of homochiral squaraine compounds acting as a highly circular dichroic active layer into conventional bulk
Elliott, R.L. et al.
Bioorganic & Medicinal Chemistry Letters, 6, 2283-2283 (1996)
M A Abreo et al.
Journal of medicinal chemistry, 39(4), 817-825 (1996-02-16)
Recent evidence indicating the therapeutic potential of cholinergic channel modulators for the treatment of central nervous system (CNS) disorders as well as the diversity of brain neuronal nicotine acetylcholine receptors (nAChRs) have suggested an opportunity to develop subtype-selective nAChR ligands

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