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Chemical Structure| 1943-67-5 Chemical Structure| 1943-67-5

Structure of 4-tert-Butylphenyl isocyanate
CAS No.: 1943-67-5

Chemical Structure| 1943-67-5

4-tert-Butylphenyl isocyanate

CAS No.: 1943-67-5

4.5 *For Research Use Only !

Cat. No.: A484735 Purity: 98%

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Product Details of [ 1943-67-5 ]

CAS No. :1943-67-5
Formula : C11H13NO
M.W : 175.23
SMILES Code : O=C=NC1=CC=C(C(C)(C)C)C=C1
MDL No. :MFCD00040718
InChI Key :WUWBDQJTQTVBSQ-UHFFFAOYSA-N
Pubchem ID :2735695

Safety of [ 1943-67-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H312-H315-H319-H332-H334-H335
Precautionary Statements:P261-P280-P305+P351+P338-P342+P311
Class:6.1
UN#:2206
Packing Group:

Application In Synthesis of [ 1943-67-5 ]

* 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 [ 1943-67-5 ]

[ 1943-67-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 32566-01-1 ]
  • [ 1943-67-5 ]
  • 1-(2-(1H-indol-2-yl)phenyl)-3-(4-tert-butylphenyl)urea [ No CAS ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; at 20℃; Example 1; 1-(2-(1H-indol-2-yl)phenyl)-3-(4-tert-butylphenyl)urea; To a solution of commercially available 2-(1H-indol-2-yl)benzenamine (62 mg, 0.3 mmol) in dichloromethane (1.5 mL) at rt was added 4-tert-butylphenyl isocyanate (30 mg, 0.171 mmol). The reaction was stirred overnight at rt. Hexane (1 mL) was added to the reaction mixture and the reaction was allowed to set for 5 min. Example 1 was the solid formed which was collected by filtration (47.3 mg). (M+H)+=384.37.
 

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