跳转至内容
Merck
CN

726796

(S)-(+)-1-环己基乙胺

ChiPros®, produced by BASF, 99%

别名:

(S)-(+)-α-甲基环己烷甲胺

登录 查看组织和合同定价。

选择尺寸


关于此项目

线性分子式:
C6H11CH(CH3)NH2
化学文摘社编号:
分子量:
127.23
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2935069
Assay:
≥98.5% (GC), 99%
Form:
liquid
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

InChI

1S/C8H17N/c1-7(9)8-5-3-2-4-6-8/h7-8H,2-6,9H2,1H3/t7-/m0/s1

SMILES string

C[C@H](N)C1CCCCC1

InChI key

XBWOPGDJMAJJDG-ZETCQYMHSA-N

assay

≥98.5% (GC), 99%

form

liquid

optical purity

enantiomeric excess: ≥98.5%

refractive index

n20/D 1.4614 (lit.)

bp

60 °C/12 mmHg (lit.)

density

0.856 g/mL at 25 °C (lit.)

functional group

amine

正在寻找类似产品? 访问 产品对比指南

General description

(S)-(+)-1-Cyclohexylethylamine is a chiral amine.

Application

(S)-(+)-1-Cyclohexylethylamine may be used in the synthesis of (S)-(-)-ferrocenylimine by reacting with ferrocenecarboxaldehyde.

Legal Information

ChiPros is a registered trademark of BASF SE

signalword

Danger

Hazard Classifications

Aquatic Chronic 2 - Flam. Liq. 3 - Skin Corr. 1B

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

125.6 °F - closed cup

flash_point_c

52 °C - closed cup

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Expedient synthesis and design strategies for new peptoid construction
Gorske, Benjamin C., et al.
Organic Letters, 7.8, 1521-1524 (2005)
Supramolecular chirogenesis in bis (zinc porphyrin): an absolute configuration probe highly sensitive to guest structure
Borovkov, Victor V., Juha M. Lintuluoto, and Yoshihisa Inoue
Organic Letters, 2.11, 1565-1568 (2000)
Isoindolinones via a room temperature palladium nanoparticle-catalysed 3-component cyclative carbonylation?amination cascade
Grigg, Ronald, et al.
Tetrahedron, 44.37, 6979-6982 (2003)
Chiral mono and diamide derivatives of calix [4] arene for enantiomeric recognition of chiral amines
Kocabas, Erdal, et al.
Chirality, 20.1, 26-34 (2008)
Yee Voan Teo et al.
Cell reports, 27(4), 997-1007 (2019-04-25)
Oncogene-induced senescence (OIS) is a tumor suppressive response to oncogene activation that can be transmitted to neighboring cells through secreted factors of the senescence-associated secretory phenotype (SASP). Currently, primary and secondary senescent cells are not considered functionally distinct endpoints. Using

商品

Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持