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Merck
모든 사진(2)

주요 문서

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M72803

Sigma-Aldrich

2-Methylpiperidine

98%

동의어(들):

α-Pipecoline, 2-Pipecoline, NSC 31047, NSC 462

로그인조직 및 계약 가격 보기

크기 선택

100 ML
₩78,663

₩78,663

출고 가능일2025년 4월 23일세부사항

벌크 견적 요청
모든 사진(2)

크기 선택

보기 변경
100 ML
₩78,663

About This Item

실험식(Hill 표기법):
C6H13N
CAS Number:
109-05-7
Molecular Weight:
99.17
Beilstein:
79804
EC Number:
203-642-1
MDL number:
MFCD00005982
UNSPSC 코드:
12352100
PubChem Substance ID:
24897152
NACRES:
NA.22

₩78,663

출고 가능일2025년 4월 23일세부사항

벌크 견적 요청

분석

98%

양식

liquid

refractive index

n20/D 1.445 (lit.)

bp

118-119 °C/753 mmHg (lit.)

density

0.844 g/mL at 25 °C (lit.)

SMILES string

CC1CCCCN1

InChI

1S/C6H13N/c1-6-4-2-3-5-7-6/h6-7H,2-5H2,1H3

InChI key

NNWUEBIEOFQMSS-UHFFFAOYSA-N

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관련 카테고리

애플리케이션

Reactant for C-2 arylation of piperidines through directed transition metal-catalyzed sp3 C-H activation[1]

Reactant for synthesis of:
  • Azepan-4-ones via two step [5+2] annulation[2]
  • 2-Aminobenzoxazoles[3]
  • Unsymmetrically substituted ureas[4]
  • Corticotropin-releasing factor receptor type 1 antagonists[5]
  • Gefitinib analogues with anti-tumor activity[6]

픽토그램

FlameSkull and crossbonesCorrosion
GHS02,GHS06,GHS05

신호어

Danger

유해 및 위험 성명서

H225,H302,H311 + H331,H314

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

50.0 °F - closed cup

Flash Point (°C)

10 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
MKCW1955
MKCR3996
MKCP0863
MKCN4961
MKCK4627

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문서 라이브러리 방문

이미 열람한 고객

Slide 1 of 2

1 of 2

Thioacetic acid 96%

Sigma-Aldrich

T30805

Thioacetic acid

Piperidine ReagentPlus®, 99%

Sigma-Aldrich

104094

Piperidine

C-2 arylation of piperidines through directed transition-metal-catalyzed sp3 C-H activation.
Hana Prokopcová et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(44), 13063-13067 (2010-10-29)
Dmitry Zuev et al.
Bioorganic & medicinal chemistry letters, 20(12), 3669-3674 (2010-05-18)
A novel series of [6-chloro-2-trifluoromethyl-7-aryl-7H-imidazo[1,2-a]imidazol-3-ylmethyl]-dialkylamines was discovered as potent CRF(1)R antagonists. The optimization of binding affinity in the series by the parallel reaction approach is discussed herein.
Xiaoqing Wu et al.
Bioorganic & medicinal chemistry, 18(11), 3812-3822 (2010-05-15)
There is an urgent need to design and develop new and more potent EGFR inhibitors with improved anti-tumor activity. Here we describe the design and synthesis of two series of 4-benzothienyl amino quinazolines as new analogues of the EGFR inhibitor
Christopher L Cioffi et al.
The Journal of organic chemistry, 75(22), 7942-7945 (2010-10-27)
The synthesis of 2-aminobenzoxazoles can be readily achieved by two versatile, one-pot procedures utilizing commercially available tetramethyl orthocarbonate or 1,1-dichlorodiphenoxymethane, an amine, and an optionally substituted 2-aminophenol. The reactions were conducted under mild conditions and provided 2-aminobenzoxazoles in modest to
Li Cui et al.
Chemical communications (Cambridge, England), 46(19), 3351-3353 (2010-05-06)
A surprisingly efficient synthesis of azepan-4-ones via a two-step [5 + 2] annulation is developed. This reaction involves a key gold catalysis and shows generally high regioselectivities and good to excellent diastereoselectivities.
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