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CS-W001157 4
Total: USD 88.00

2-Amino-6-methoxybenzothiazole

  • CAS No. 1747-60-0

  • Cat. No. CS-D1441
  • Molecule weight180.23
  • Purity≥96%
  • MDL No.MFCD00005787

*For research and further manufacturing use only, not for direct human use.

2-Amino-6-methoxybenzothiazole|CS-D1441

Structure of 1747-60-0

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General Information

  • CAS No. 1747-60-0
  • Cat. No. CS-D1441
  • Purity ≥96%
  • MDL No. MFCD00005787
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₈N₂OS
  • Molecular Weight 180.23
  • Synonym(s) 6-Methoxy-2-aminobenzothiazole; 6-Methoxy-2-benzothiazolamine; 6-Methoxybenzo[d]thiazol-2-amine; NSC 27516; 6-methoxybenzothiazol-2-ylamine
  • SMILES NC1=NC2=CC=C(OC)C=C2S1

Description

2-Amino-6-methoxybenzothiazole undergoes Sandmeyer reaction on heating with isoamyl nitrite and CuBr2 to yield 2-bromo-6-methoxybenzothiazole.2-Amino-6-methoxybenzothiazole was used as building block in the syntheses of novel series of Schiff bases and 4-thiazolidinones. It was used in the synthesis of 2-cyano-6-methoxybenzothiazole, key intermediate for the synthesis of firefly luciferin.

Synthesis

  • Route1
    • null|null
      333-20-0
    • null|null
      104-94-9
    • ~95%
    • In-stock
      2-Amino-6-methoxybenzothiazole|CS-D1441
      1747-60-0

    References

    • Synlett, , vol. 23, # 15 p. 2219 - 2222
  • Route2
    • null|null
      1147550-11-5
    • null|null
      104-94-9
    • ~94%
    • In-stock
      2-Amino-6-methoxybenzothiazole|CS-D1441
      1747-60-0

    References

    • Synlett, , # 19 p. 2952 - 2956
  • Route3

    References

    • Helvetica Chimica Acta, , vol. 63, # 3 p. 682 - 692

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   48.14
  • LogP   1.8871
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   1

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