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Chemical Structure| 76014-12-5 Chemical Structure| 76014-12-5

Structure of 76014-12-5

Chemical Structure| 76014-12-5

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Product Details of [ 76014-12-5 ]

CAS No. :76014-12-5
Formula : C10H17ClN2O
M.W : 216.71
SMILES Code : [H]Cl.NNC1=CC=C(OCCCC)C=C1

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Application In Synthesis of [ 76014-12-5 ]

* 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 [ 76014-12-5 ]

[ 76014-12-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 76014-12-5 ]
  • [ 104618-32-8 ]
  • 3-amino-6-n-butyloxy-1,2,3,4-tetrahydrocarbazole oxalate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With oxalic acid; EXAMPLE 14 3-Amino-6-n-butyloxy-1,2,3,4-tetrahydrocarbazole oxalate Reaction of <strong>[104618-32-8]4-phthalimidocyclohexanone</strong> (1.12 g) with 4-n-butyloxyphenyl hydrazine hydrochloride (1.00 g) and subsequent deprotection by the method described in example 3, gave the title compound free base. This was treated with oxalic acid to give the oxalate salt (0.47 g), mp 227-229 C.
With oxalic acid; Example 14 3-Amino-6-n-butyloxy-1,2,3,4-tetrahydrocarbazole oxalate Reaction of <strong>[104618-32-8]4-phthalimidocyclohexanone</strong> (1.12 g) with 4-n-butyloxyphenyl hydrazine hydrochloride (1.00 g) and subsequent deprotection by the method described in example 3, gave the title compound free base. This was treated with oxalic acid to give the oxalate salt (0.47 g), mp 227-229 C.
With oxalic acid; Example 14 3-Amino-6-n-butyloxy-1,2,3,4-tetrahydrocarbazole oxalate Reaction of <strong>[104618-32-8]4-phthalimidocyclohexanone</strong> (1.12 g) with 4-n-butyloxyphenyl hydrazine hydrochloride (1.00 g) and subsequent deprotection by the method described in example 3, gave the title compound free base. This was treated with oxalic acid to give the oxalate salt (0.47 g), mp 227 - 229C.
 

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