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4-Methoxyphenyl isothiocyanate, 98%
4-Methoxyphenyl isothiocyanate, 98%
4-Methoxyphenyl isothiocyanate, 98%
Thermo Scientific Chemicals

4-Methoxyphenyl isothiocyanate, 98%

CAS: 2284-20-0 | C8H7NOS | 165.21 g/mol
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数量:
2 g
10 g
50 g
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製品番号（カタログ番号） A15331.04
または、製品番号A15331-04
価格（JPY）
-
数量:
2 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS2284-20-0
IUPAC Name1-isothiocyanato-4-methoxybenzene
Molecular FormulaC8H7NOS
InChI KeyVRPQCVLBOZOYCG-UHFFFAOYSA-N
SMILESCOC1=CC=C(C=C1)N=C=S
さらに表示
仕様Specification Sheetスペックシート
Appearance (Color)Clear colorless to yellow
FormLiquid
Assay (GC)≥97.5%
Refractive Index1.6470-1.6510 @ 20?C
4-Methoxyphenyl isothiocyanate has been used in the synthesis of 3-benzyl-2-(4-methoxyphenyl)-3H-[1,2,4]triazolo-[5,1-b]quinazolin-9-one and 2-{[4-amino-3-(4-methylphenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]acetyl}-N-arylhydrazinecarbothioamides.

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
4-Methoxyphenyl isothiocyanate has been used in the synthesis of 3-benzyl-2-(4-methoxyphenyl)-3H-[1,2,4]triazolo-[5,1-b]quinazolin-9-one and 2-{[4-amino-3-(4-methylphenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]acetyl}-N-arylhydrazinecarbothioamides.

Solubility
It hydrolyzes in water.

Notes
Moisture sensitive. Incompatible with oxidizing agents, alcohols and amines.
RUO – Research Use Only

General References:

  1. Veerachamy Alagarsamya; Urvishbhai S.Pathak. Synthesis and antihypertensive activity of novel 3-benzyl-2-substituted-3H-[1,2,4]triazolo[5,1-b]quinazolin-9-ones. Bioorganic & Medicinal Chemistry. 2007, 15,(10), 3457-3462.
  2. Ahmet Demirbas; Deniz Sahin; Neslihan Demirbas; Sengül Alpay Karaoglu; Ahmet Demirbas; Deniz Sahin; Neslihan Demirbas; Sengül Alpay Karaoglu. Synthesis of some new 1,3,4-thiadiazol-2-ylmethyl-1,2,4-triazole derivatives and investigation of their antimicrobial activities. European Journal of Medicinal Chemistry. 2009, 44,(7), 2896-2903.