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Merck
모든 사진(3)

주요 문서

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497312

Sigma-Aldrich

4-Piperidinemethanol

97%

동의어(들):

4-(Hydroxymethyl)piperidine

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모든 사진(3)

About This Item

실험식(Hill 표기법):
C6H13NO
CAS Number:
6457-49-4
Molecular Weight:
115.17
MDL number:
MFCD00174228
UNSPSC 코드:
12352100
PubChem Substance ID:
24873109
NACRES:
NA.22

Quality Level

100

분석

97%

bp

118-120 °C/10 mmHg (lit.)

mp

55-59 °C (lit.)

작용기

hydroxyl

SMILES string

OCC1CCNCC1

InChI

1S/C6H13NO/c8-5-6-1-3-7-4-2-6/h6-8H,1-5H2

InChI key

XBXHCBLBYQEYTI-UHFFFAOYSA-N

관련 카테고리

일반 설명

4-Piperidinemethanol is a cyclic secondary amine. Its standard molar enthalpies of combustion, sublimation and formation have been determined.

애플리케이션

4-Piperidinemethanol may be used in the preparation of:
  • N-tert-butoxycarbonyl-4-hydroxymethyl piperidine
  • desferrioxamine B (DFO) containing third generation triazine dendrimer
  • ethyl 3-(4-(hydroxymethyl)piperidin-1-yl)propanoate (EHMPP)
  • 4-(hydroxymethyl)piperidine-1-carbodithioic acid (HL)
  • 1-[[(1E)-2-(4-chlorophenyl)ethenyl]sulfonyl]-4-piperidinemethanol
Substrate used in solid-phase organic synthesis of a secondary amine.

픽토그램

Corrosion
GHS05

신호어

Danger

유해 및 위험 성명서

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point (°F)

230.0 °F - closed cup

Flash Point (°C)

110 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
SHBK8917
SHBC0677V
SHBC0676V
42996DJ
06227PH

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3-Methylamino-1-propanol 96%

Sigma-Aldrich

715662

3-Methylamino-1-propanol

Ethyl isonipecotate 98%

Sigma-Aldrich

E33505

Ethyl isonipecotate

4-Pyridinemethanol 99%

Sigma-Aldrich

151629

4-Pyridinemethanol

Jongdoo Lim et al.
Bioorganic & medicinal chemistry, 18(15), 5749-5753 (2010-07-10)
The synthesis of a third generation triazine dendrimer, 1, containing multiple, iron-sequestering desferrioxamine B (DFO) groups is described. Benzoylation of the hydroxamic acid groups of DFO and formation of a reactive dichlorotriazine provide the intermediate for reaction with the second
Enzymatic synthesis, thermal and crystalline properties of a poly (β-amino ester) and poly (lactone-co-β-amino ester) copolymers.
Martino L, et al.
Polymer, 53(9), 1839-1848 (2012)
Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as factor Xa inhibitor.
Nishida H, et al.
Chemical & Pharmaceutical Bulletin, 49(10), 1237-1244 (2001)
Christian A Olsen et al.
Organic letters, 6(12), 1935-1938 (2004-06-05)
[reaction: see text] An expedient solid-phase synthetic approach to secondary and tertiary amines was developed. The protocol employs conversion of resin-bound amino alcohols to the corresponding iodides, followed by iodide displacement with primary or secondary amines or with unprotected amino
Synthesis, spectroscopy, and biological activity of heterobimetallic complexes containing Sn (IV) and Pd (II) with 4-(hydroxymethyl) piperidine-1-carbodithioic acid.
Anwar MT, et al.
Russ. J. Gen. Chem., 83(12), 2380-2385 (2013)
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