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Chemical Structure| 1244041-71-1 Chemical Structure| 1244041-71-1

Structure of 1244041-71-1

Chemical Structure| 1244041-71-1

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Product Details of [ 1244041-71-1 ]

CAS No. :1244041-71-1
Formula : C12H13BrN2O2S
M.W : 329.21
SMILES Code : O=C(OC(C)(C)C)NC1=NC2=CC=C(Br)C=C2S1
MDL No. :MFCD16036619
InChI Key :BIRRUNIKTIVYSQ-UHFFFAOYSA-N
Pubchem ID :77231294

Safety of [ 1244041-71-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362

Application In Synthesis of [ 1244041-71-1 ]

* 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 [ 1244041-71-1 ]

[ 1244041-71-1 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 1244041-71-1 ]
  • [ 1171892-42-4 ]
  • C15H15N3OS [ No CAS ]
  • 2
  • [ 1244041-71-1 ]
  • [ 1171892-42-4 ]
  • C20H23N3O3S [ No CAS ]
  • 3
  • [ 1244041-71-1 ]
  • [ 1151802-22-0 ]
  • C18H20N4O2S [ No CAS ]
  • 4
  • [ 1244041-71-1 ]
  • [ 1151802-22-0 ]
  • C13H12N4S [ No CAS ]
  • 5
  • [ 1244041-71-1 ]
  • [ 20358-03-6 ]
  • [ 1160573-06-7 ]
YieldReaction ConditionsOperation in experiment
94% Step 1: tert-Butyl 5-bromobenzo[d]thiazol-2-ylcarbamate The title compound (25.1 g, 94% yield) was generated from <strong>[20358-03-6]5-bromobenzo[d]thiazol-2-amine</strong> (18.4 g, 80.3 mmol) following a procedure analogous to Example 214, step 1. LCMS (ESI): [M+H]+=329/331.
 

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Technical Information

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Related Functional Groups of
[ 1244041-71-1 ]

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Related Parent Nucleus of
[ 1244041-71-1 ]

Benzothiazoles

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