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Merck
CN

429058

Sigma-Aldrich

2-氟乙胺 盐酸盐

technical grade, 90%

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About This Item

线性分子式:
FCH2CH2NH2 · HCl
CAS号:
分子量:
99.54
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

等级

technical grade

质量水平

方案

90%

表单

solid

mp

99-103 °C (lit.)

官能团

amine
fluoro

SMILES字符串

Cl.NCCF

InChI

1S/C2H6FN.ClH/c3-1-2-4;/h1-2,4H2;1H

InChI key

YRRZGBOZBIVMJT-UHFFFAOYSA-N

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一般描述

2-Fluoroethylamine hydrochloride is a fluorinated alkylammonium salt. Studies suggest that adding a fluorine atom to it leads to double gauche effect in the resulting 2,2-difluoroethylamine chloride. Microwave spectral studies for 2-fluoroethylamine has been conducted.

应用

2-Fluoroethylamine hydrochloride may be used in the synthesis of the following:
  • 2-fluoroethylisocyanate
  • 1,3-bis-(2-fluoroethyl) urea (BFU)
  • N-2-fluoroethylmaleimide
  • [Cu4(O)(Ln)2(CH3COO)4] where HL= 4-methyl-2,6-bis(2-fluoroethyliminomethyl) phenol
  • 1-O-(4-(2-fluoroethyl-carbamoyloxymethyl)-2-nitrophenyl)-O-β-D-glucopyronuronate (FEAnGA)

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

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访问文档库

Development of a new thiol site-specific prosthetic group and its conjugation with [Cys40]-exendin-4 for in vivo targeting of insulinomas.
Yue X, et al.
Bioconjugate Chemistry, 24(7), 1191-1200 (2013)
Conformational analysis of 2, 2-difluoroethylamine hydrochloride: double gauche effect.
Silla JM, et al.
Beilstein Journal of Organic Chemistry, 10(1), 877-882 (2014)
Inês F Antunes et al.
Bioconjugate chemistry, 21(5), 911-920 (2010-04-27)
To increase the therapeutic index of chemotherapeutic drugs, prodrugs have been investigated as anticancer agents, as they may present fewer cytotoxic side effects than conventional cytotoxic drugs, while therapeutic efficacy is maintained or even increased. Extracellular beta-glucuronidase (beta-GUS) in the
Synthesis of 18F-labelled 2-fluoroethyl-nitrosoureas.
Farrokhzad S, et al.
Canadian Journal of Chemistry, 62(11), 2107-2112 (1984)
Tetranuclear copper (II)-Schiff-base complexes as active catalysts for oxidation of cyclohexane and toluene.
Roy P and Manassero M.
Dalton Transactions, 39(6), 1539-1545 (2010)

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