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Merck
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190241

Sigma-Aldrich

2-氨基-6-硝基苯并噻唑

≥97%

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About This Item

經驗公式(希爾表示法):
C7H5N3O2S
CAS號碼:
分子量::
195.20
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

≥97%

mp

247-249 °C (lit.)

SMILES 字串

Nc1nc2ccc(cc2s1)[N+]([O-])=O

InChI

1S/C7H5N3O2S/c8-7-9-5-2-1-4(10(11)12)3-6(5)13-7/h1-3H,(H2,8,9)

InChI 密鑰

GPNAVOJCQIEKQF-UHFFFAOYSA-N

一般說明

用直流电伏安法和微分脉冲伏安法研究了2-氨基-6-硝基苯并噻唑的伏安行为

應用

2-氨基-6-硝基苯并噻唑用于:
  • 伏安法测定电化学可还原有机物的模型分析物
  • 2-甲基-4-硝基-2H-吡唑-3-羧酸[2-(环己烷羰基氨基)苯并噻唑-6-基]酰胺衍生物的合成
  • 含有噻唑和苯并噻唑受体的推挽式非线性光学发色团的制备
  • 作为重氮化反应生产染料的基础

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


分析證明 (COA)

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Masao Yoshida et al.
Bioorganic & medicinal chemistry letters, 15(14), 3328-3332 (2005-06-16)
Based on 2-methyl-4-nitro-2H-pyrazole-3-carboxylic acid[2-(cyclohexanecarbonylamino)benzothiazol-6-yl]amide (1), which shows selective cytotoxicity against tumorigenic cell lines, 2,6-dichloro-N-[2-(cyclopropanecarbonylamino)benzothiazol-6-yl]benzamide (13b) was designed and synthesized as a biologically stable derivative containing no nitro group. The highly potent derivative 13b exhibited excellent in vivo inhibitory effect on
Synthesis and characterization of thermally stable second-order nonlinear optical side-chain polyimides containing thiazole and benzothiazole push-pull chromophores.
Tambe SM, et al.
Opt. Mater., 31(6), 817-825 (2009)
Voltammetric determination of 2-amino-6-nitrobenzothiazole at two different silver amalgam electrodes.
Deylova D, et al.
Electrochimica Acta, 62, 335-340 (2012)
Dana Deýlová et al.
Talanta, 102, 68-74 (2012-11-28)
New type of bismuth film electrode prepared by electrodeposition of bismuth film on a silver solid amalgam substrate (BiF-AgSAE) was tested as a sensor for voltammetric determination of electrochemically reducible organic substances using 2-amino-6-nitrobenzothiazole (ANBT) as a model analyte. Using

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