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Merck
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232270

Sigma-Aldrich

3-Amino-5-methylisoxazole

≥97%

동의어(들):

5-Methyl-3-isoxazolamine, NSC 159134

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50 G
₩226,244

₩226,244

예상 입고일2025년 4월 21일세부사항

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모든 사진(1)

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50 G
₩226,244

About This Item

실험식(Hill 표기법):
C4H6N2O
CAS Number:
1072-67-9
Molecular Weight:
98.10
Beilstein:
108110
EC Number:
214-013-6
MDL number:
MFCD00003155
UNSPSC 코드:
12352100
PubChem Substance ID:
24853889
NACRES:
NA.22

₩226,244

예상 입고일2025년 4월 21일세부사항

벌크 견적 요청

Quality Level

200

분석

≥97%

양식

solid

mp

59-61 °C (lit.)

SMILES string

Cc1cc(N)no1

InChI

1S/C4H6N2O/c1-3-2-4(5)6-7-3/h2H,1H3,(H2,5,6)

InChI key

FKPXGNGUVSHWQQ-UHFFFAOYSA-N

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관련 카테고리

일반 설명

3-Amino-5-methylisoxazole is the major intermediate formed during sulfamethoxazole biodegradation by Pseudomonas psychrophila strain HA-4[1]. It is the intermediate formed during the photocatalytic degradation of sulfamethoxazole (SMX)[2].

애플리케이션

3-Amino-5-methylisoxazole was used in synthesis of:
  • naphtho[1,2-e][1,3]oxazines[3]
  • series of 1-aryl-4-methyl-3,6-bis-(5-methylisoxazol-3-yl)-2-thioxo-2,3,6,10b-tetrahydro-1H-pyrimido[5,4-c]quinolin-5-ones, having potential mosquito larvicidal activity[4]
  • hydroxylamines of sulfadiazine and sulfamethoxazole[5]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

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시험 성적서(COA)

Lot/Batch Number
WXBF1628V
BCCJ4312
BCCC4672
BCBV0221
BCBT7302

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이미 열람한 고객

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2-Aminopyrimidine 97%

Sigma-Aldrich

A78608

2-Aminopyrimidine

2-Aminothiazole 97%

Sigma-Aldrich

123129

2-Aminothiazole

Mehdi Shafiee et al.
Molecular diversity, 16(4), 727-735 (2012-10-24)
An expeditious, straightforward and efficient synthesis of diversely naphtho[1,2-e][1,3]oxazines via one-pot condensation reaction of β- naphthol, 3-amino-5-methylisoxazole and arylaldehydes catalyzed by bismuth(III) trifluoromethanesulfonate is described. The reaction preferentially afforded 1,3-trans oxazines.
Shiyuan Ding et al.
Journal of hazardous materials, 262, 812-818 (2013-10-22)
Photocatalytic degradation of sulfamethoxazole (SMX) was investigated using Bi2O3/Bi2O2CO3/Sr6Bi2O9 (BSO) photocatalyst under visible light (>420 nm) irradiation. The photochemical degradation of SMX followed pseudo-first-order kinetics. The reaction kinetics was determined as a function of initial SMX concentrations (5-20 mg L(-1))
Benchao Jiang et al.
Applied microbiology and biotechnology, 98(10), 4671-4681 (2014-02-14)
Sulfamethoxazole is a common antibiotic that is frequently detected in wastewater and surface water. This study investigated the biodegradation and metabolic pathway of sulfamethoxazole by Pseudomonas psychrophila HA-4, a cold-adapted bacterium. Strain HA-4, which uses sulfamethoxazole as its sole source
Lu Wang et al.
Water research, 88, 322-328 (2015-10-30)
Sulphamethoxazole (SMX) is extensively used in humans and livestock, but its appearance in natural water raises environmental concerns. This study demonstrated that SMX and its degradation product, 3-amino-5-methylisoxazole (3A5MI), could be effectively degraded in microbial fuel cell (MFC) reactors. Approximately
Yan Li et al.
The Science of the total environment, 633, 1217-1226 (2018-05-16)
Sulfamethoxazole (SMX) is a sulfonamide antibiotic, widely used as curative and preventive drug for human, animal, and aquaculture bacterial infections. Its residues have been ubiquitously detected in the surface waters and sediments. In the present study, SMX dissipation and kinetics
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