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Chemical Structure| 7149-10-2 Chemical Structure| 7149-10-2
Chemical Structure| 7149-10-2

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Synonyms: Vanillylamine hydrochloride

4.5 *For Research Use Only !

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Product Details of Vanillylamine HCl

CAS No. :7149-10-2
Formula : C8H12ClNO2
M.W : 189.64
SMILES Code : OC1=CC=C(CN)C=C1OC.[H]Cl
Synonyms :
Vanillylamine hydrochloride
MDL No. :MFCD00012864
InChI Key :PUDMGOSXPCMUJZ-UHFFFAOYSA-N
Pubchem ID :165576

Safety of Vanillylamine HCl

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Vanillylamine HCl

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 7149-10-2 ]

[ 7149-10-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7149-10-2 ]
  • [ 426463-05-0 ]
  • 4-(((5-iodo-3-nitropyridin-2-yl)amino)methyl)-2-methoxyphenol [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 100℃; for 1.0h; Example 3-57-1 Preparation of 4-(((5-iodo-3-nitropyridin-2-yl)amino)methyl)-2-methoxyphenol To a stirred suspension of 4-hydroxy-3-methoxybenzylamine hydrochloride (1.32 g, 6.82 mmol) and <strong>[426463-05-0]2-chloro-5-iodo-3-nitropyridine</strong> (2.00 g, 6.82 mmol) in acetonitrile (20 mL) was added N,N-disopropylethylamine (5.96 ml, 34.10 mmol) The suspension was stirred and heated to 100 C. After 1 h, the mixture was allowed to cool to room temperature, and 2N aqueous potassium hydroxide solution (0.68 mL) was added. The mixture was concentrated to provide 4-(((5-iodo-3-nitropyridin-2-yl)amino)methyl)-2-methoxyphenol as an impure solid.
 

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