3,4-Dihydro-2H-1,4-benzoxazine, 97%
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3,4-Dihydro-2H-1,4-benzoxazine, 97%
3,4-Dihydro-2H-1,4-benzoxazine, 97%
3,4-Dihydro-2H-1,4-benzoxazine, 97%
Thermo Scientific Chemicals

3,4-Dihydro-2H-1,4-benzoxazine, 97%

CAS: 5735-53-5 | C8H9NO | 135.166 g/mol
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数量:
1 g
5 g
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製品番号（カタログ番号） H33641.03
または、製品番号H33641-03
価格（JPY）
-
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数量:
1 g
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化学物質識別子
CAS5735-53-5
IUPAC Name3,4-dihydro-2H-1,4-benzoxazine
Molecular FormulaC8H9NO
InChI KeyYRLORWPBJZEGBX-UHFFFAOYSA-N
SMILESC1COC2=CC=CC=C2N1
さらに表示
仕様Specification Sheetスペックシート
FormLiquid
Refractive Index1.5940-1.5990 @ 20?C
Assay (GC)≥96.0%
Appearance (Color)Clear pale yellow to yellow
It is used as pharmaceutical intermediate. Benzoylthiophenes are allosteric enhancers (AE) of agonist activity at the A1 adenosine receptor.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is used as pharmaceutical intermediate. Benzoylthiophenes are allosteric enhancers (AE) of agonist activity at the A1 adenosine receptor.

Solubility
Sparingly soluble in water.(0.26 g/L) (25°C),

Notes
Store in cool dry place. Ensure proper ventilation. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. C. Elisabet Tranberg.; Andrea Zickgraf.; Brian N. Giunta.; Henning Luetjens.; Heidi Figler.; Lauren J. Murphree.; Ruediger Falke.; Holger Fleischer.; Joel Linden.; Peter J. Scammells.; Ray. A. Olsson. 2-Amino-3-aroyl-4,5-alkylthiophenes:  Agonist Allosteric Enhancers at Human A1 Adenosine Receptors.J. Med. Chem. 2002, 45 (2),382-389 .
  2. Robert H. Dodd.; Catherine Ouannes.; Malka Robert-Gero.; Pierre Potier. Hybrid molecules: growth inhibition of Leishmania donovani promastigotes by thiosemicarbazones of 3-carboxy-.beta.-carbolines.J. Med. Chem. 1989, 32 (6),1272-1276 .