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1201187-44-1

Carbamic acid, N-[5-[(4-methylphenyl)sulfonyl]-5H-pyrrolo[2,3-b]pyrazin-2-yl]-, 1,1-dimethylethyl ester

Catalog#: AR000R12  |   CAS#: 1201187-44-1  |   MDL#: MFCD28129728  |   MF: C18H20N4O4S  |   MW: 388.4408

Packsize Purity Price Availability Quantity
1g 98% $11.00 Global Stock Buy Now Add To Cart
5g 98% $35.00 Global Stock Buy Now Add To Cart
10g 98% $59.00 Global Stock Buy Now Add To Cart
25g 98% $118.00 Global Stock Buy Now Add To Cart
50g 98% $200.00 Global Stock Buy Now Add To Cart
100g 98% $315.00 Global Stock Buy Now Add To Cart
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Catalog Number AR000R12
Chemical Name Carbamic acid, N-[5-[(4-methylphenyl)sulfonyl]-5H-pyrrolo[2,3-b]pyrazin-2-yl]-, 1,1-dimethylethyl ester
CAS Number 1201187-44-1
Molecular Formula C18H20N4O4S
Molecular Weight 388.4408
MDL Number MFCD28129728
SMILES O=C(OC(C)(C)C)Nc1cnc2c(n1)ccn2S(=O)(=O)c1ccc(cc1)C

A key application of tert-Butyl (5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)carbamate in chemical synthesis lies in its potential as a versatile building block for the creation of complex organic molecules. This compound serves as a strategic precursor for the synthesis of various biologically active compounds, pharmaceutical intermediates, and functional materials. By utilizing the unique reactivity and structural characteristics of this molecule, chemists can efficiently introduce specific functionalities and stereochemical features into target molecules, enabling the synthesis of novel compounds with tailored properties and activities. The tert-Butyl (5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)carbamate can participate in a range of synthetic transformations, including cross-coupling reactions, cyclization processes, and functional group manipulations, offering a valuable tool for designing and constructing molecular structures with precision and control.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H317
Precautionary Statements P280
Class N/A
Packing Group N/A

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