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Chemical Structure| 59134-95-1 Chemical Structure| 59134-95-1

Structure of 59134-95-1

Chemical Structure| 59134-95-1

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Product Details of [ 59134-95-1 ]

CAS No. :59134-95-1
Formula : C3H5ClN2S
M.W : 136.60
SMILES Code : NC1=CSC=N1.[H]Cl
MDL No. :MFCD18072469
InChI Key :QBBARGGAFRDZBC-UHFFFAOYSA-N
Pubchem ID :68841472

Safety of [ 59134-95-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501

Application In Synthesis of [ 59134-95-1 ]

* 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 [ 59134-95-1 ]

[ 59134-95-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1235406-42-4 ]
  • [ 59134-95-1 ]
YieldReaction ConditionsOperation in experiment
99% With hydrogenchloride; In 1,4-dioxane; dichloromethane; water; at 20℃; for 3h; Step 1. Preparation of thiazol-4-amine hydrochloride To a mixture of <strong>[1235406-42-4]tert-butyl thiazol-4-ylcarbamate</strong> (34.0 g, 169.8 mmol) in dichloromethane (150 mL) was added 4.0 M hydrochloric acid in anhydrous dioxane (180 mL). The reaction mixture was stirred at ambient temperature for 3 hours and then filtered. The residue rinsed with diethyl ether (80 mL) to afford the title compound as a colorless solid (22.99 g, 99% yield): MS (ES+) m/z 101 (M+1).
 

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