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C1=CC(=CC=C1O)SC2=C(C=C(C=C2)O)NChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 3-amino-4-(4-hydroxyphenyl)sulfanylphenol |
|---|---|
| IUPAC Name | — |
| CAS Number | 943774-28-5 |
| Database ID | 67040301 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
3-amino-4-(4-hydroxyphenyl)sulfanylphenol (CAS 943774-28-5) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
Potential Applications
For professional research and industrial use only
Database ID 67040301
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
12 reactions · 12 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-1f12c4f3fa29470d9b9c7b0911e0904bConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The product of Example 48B (380 mg, 1.63 mmol) was reacted with the product of Example 15A (284 mg, 1.63 mmol) using the procedure of Example 15E substituting the product of Example 48B for the product of Example 15D to provide a solid which was triturated with methanol to provide the title compound (209 mg, 35%). to provide a solid which was triturated with methanol
Source ID: ord-48658e87e4e14f8a8d5f6ec4b419f02cConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The product from Example 48A (1.34 g, 5.09 mmol) was reacted with iron (1.42 g, 25.48 mmol) and ammonium chloride (409 mg, 1.5 mmol) in 20 mL EtOH/20 ml, THF/6 mL water following the procedure from Example 10E to provide the title compound (1.168 g, 97%).
Source ID: ord-96ffba23fe7243768eedc6596809cbebConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The product of Example 16B (380 mg, 1.63 mmol) was reacted with the product of Example 15A (284 mg, 1.63 mmol) using the procedure of Example 15E substituting the product of Example 16B for the product of Example 15D to provide a solid which was triturated with methanol to provide the title compound (209 mg, 35%). to provide a solid which was triturated with methanol
Source ID: ord-7d933d83cff84ce6b090c50c1425ffb0Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The product of Example 16B (380 mg, 1.63 mmol) was reacted with the product of Example 15A (284 mg, 1.63 mmol) using the procedure of Example 15E substituting the product of Example 16B for the product of Example 15D to provide a solid which was triturated with methanol to provide the title compound (209 mg, 35%). to provide a solid which was triturated with methanol
Source ID: ord-7d933d83cff84ce6b090c50c1425ffb0Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The product from Example 16A (1.34 g, 5.09 mmol) was reacted with iron (1.42 g, 25.48 mmol) and ammonium chloride (409 mg, 1.5 mmol) in 20 mL EtOH/20 mL THF/6 mL water following the procedure from Example 10E to provide the title compound (1.168 g, 97%).
Source ID: ord-52d5ccbf76434193a95310af8d387c25Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The product of Example 153B (380 mg, 1.63 mmol) was reacted with the product of Example 29A (284 mg, 1.63 mmol) using the procedure of Example 29E substituting the product of Example 153B for the product of Example 29D to provide a solid which was triturated with methanol to provide the title compound (209 mg, 35%). to provide a solid which was triturated with methanol
Source ID: ord-efc23e559d5d4fcfa8ede741eae2a5a9Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The product from Example 153A (1.34 g, 5.09 mmol) was reacted with iron (1.42 g, 25.48 mmol) and ammonium chloride (409 mg, 1.5 mmol) in 20 mL EtOH/20 mL THF/6 mL water following the procedure from Example 9E to provide the title compound (1.168 g, 97%).
Source ID: ord-d367880a7bc94cf1b0a8578927c5c122Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The product from Example 153A (1.34 g, 5.09 mmol) was reacted with iron (1.42 g, 25.48 mmol) and ammonium chloride (409 mg, 1.5 mmol) in 20 mL EtOH/20 mL THF/6 mL water following the procedure from Example 9E to provide the title compound (1.168 g, 97%).
Source ID: ord-d367880a7bc94cf1b0a8578927c5c122Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-1f12c4f3fa29470d9b9c7b0911e0904bConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The product of Example 48B (380 mg, 1.63 mmol) was reacted with the product of Example 15A (284 mg, 1.63 mmol) using the procedure of Example 15E substituting the product of Example 48B for the product of Example 15D to provide a solid which was triturated with methanol to provide the title compound (209 mg, 35%). to provide a solid which was triturated with methanol
Source ID: ord-48658e87e4e14f8a8d5f6ec4b419f02cConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The product from Example 48A (1.34 g, 5.09 mmol) was reacted with iron (1.42 g, 25.48 mmol) and ammonium chloride (409 mg, 1.5 mmol) in 20 mL EtOH/20 ml, THF/6 mL water following the procedure from Example 10E to provide the title compound (1.168 g, 97%).
Source ID: ord-96ffba23fe7243768eedc6596809cbebPubChem References
These sources are listed in the compound's public database record.
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