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424218

Sigma-Aldrich

3-氨基异噁唑

95%

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About This Item

经验公式（希尔记法）:
C3H4N2O
CAS号:
1750-42-1
分子量:
84.08
MDL號碼:
MFCD00038814
分類程式碼代碼:
12352100
PubChem物質ID:
24866558
NACRES:
NA.22

品質等級

100

化驗

95%

形狀

liquid

折射率

n20/D 1.511 (lit.)

bp

226-228 °C (lit.)

密度

1.138 g/mL at 25 °C (lit.)

SMILES 字串

Nc1ccon1

InChI

1S/C3H4N2O/c4-3-1-2-6-5-3/h1-2H,(H2,4,5)

InChI 密鑰

RHFWLPWDOYJEAL-UHFFFAOYSA-N

相关类别

一般說明

3-Aminoisoxazole (isoxazol-3-amine) is a 3-substituted isoxazole derivative. It is a structural isomer of 5-aminoisoxazole.

應用

3-Aminoisoxazole (isoxazol-3-amine) may be used in the following studies:
  • As a reagent in the synthesis of N-(4-(N-isoxazol-3-ylsulfamoyl)phenyl)acetamide.
  • As a starting material in the synthesis of N-(isoxazol-3-yl)-N′-(carbomethoxy)thiourea.
  • As a starting material in the synthesis of (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxy-iminoacetic acid, a side-chain of the fourth generation of cephem antibiotics.

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315 - H319 - H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

235.4 °F

閃點（°C）

113 °C

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Sigma-Aldrich

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Synthesis of 3-and 5-amino-5-(3)-(pyrrol-2-yl) isoxazoles.
Lyubov'N S, et al.
Tetrahedron, 61(20), 4841-4849 (2005)
Martin J. Walsh et al.
Probe Reports from the NIH Molecular Libraries Program, 2011 Oct 18 (Updated 2013 Feb 25) (2013-09-13)
The protist
Tomasz Glinka et al.
Bioorganic & medicinal chemistry, 11(4), 591-600 (2003-01-23)
SAR studies in a series of related 3-(heteroarylthio)cephems determined that a relatively high chemical reactivity of the beta-lactam ring, modulated by electronic effects of substituents at C-3 and C-7, is necessary to achieve high in vitro activity against methicillin-resistant Staphylococcus
Kuniaki Tatsuta
Proceedings of the Japan Academy. Series B, Physical and biological sciences, 84(4), 87-106 (2008-10-23)
The first total synthesis and development of a variety of bioactive natural products have been accomplished by using carbohydrates as a chiral source. In addition, practically useful intermediates have been created, analogs of natural products have been prepared, their structure-activity

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