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125414-41-7

Carbamic acid, N-[2-hydroxy-1-(hydroxymethyl)ethyl]-, 1,1-dimethylethyl ester

Catalog#: AR000OCU  |   CAS#: 125414-41-7  |   MDL#: MFCD00270213  |   MF: C8H17NO4  |   MW: 191.2249

Packsize Purity Price Availability Quantity
250mg 97% $4.00 Global Stock Buy Now Add To Cart
1g 97% $4.00 Global Stock Buy Now Add To Cart
5g 97% $12.00 Global Stock Buy Now Add To Cart
10g 97% $21.00 Global Stock Buy Now Add To Cart
25g 97% $45.00 Global Stock Buy Now Add To Cart
100g 97% $139.00 Global Stock Buy Now Add To Cart
250g 97% $208.00 Global Stock Buy Now Add To Cart
500g 97% $312.00 Global Stock Buy Now Add To Cart
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Catalog Number AR000OCU
Chemical Name Carbamic acid, N-[2-hydroxy-1-(hydroxymethyl)ethyl]-, 1,1-dimethylethyl ester
CAS Number 125414-41-7
Molecular Formula C8H17NO4
Molecular Weight 191.2249
MDL Number MFCD00270213
SMILES OCC(NC(=O)OC(C)(C)C)CO

Tert-Butyl (1,3-dihydroxypropan-2-yl)carbamate, also known as $name$, serves as a valuable reagent in chemical synthesis processes. Its unique structure and properties make it a versatile compound with various applications in the lab.In chemical synthesis, $name$ is commonly used as a protecting group for hydroxyl functionalities in organic molecules. By selectively masking hydroxyl groups with $name$, chemists can prevent unwanted reactions or side reactions from occurring at these sites during the synthesis of complex molecules. This protective group strategy allows for greater control over reaction pathways and facilitates the synthesis of target compounds with multiple hydroxyl groups.Another important application of $name$ is in the preparation of carbamate derivatives. The presence of both a carbamate and hydroxyl functionalities in $name$ enables chemists to access a wide range of carbamate-containing compounds through various synthetic transformations. These derivatives can exhibit diverse functionalities and play crucial roles in medicinal chemistry, materials science, and agrochemical research.Additionally, the tert-butyl group in $name$ provides steric hindrance, which can influence the reactivity and selectivity of reactions involving the carbamate moiety. By tuning the steric environment around the carbamate group, chemists can fine-tune the properties of the target molecules and control their behavior in biological systems or material applications.Overall, the application of tert-Butyl (1,3-dihydroxypropan-2-yl)carbamate in chemical synthesis enables chemists to design and access a wide range of functionalized compounds with tailored properties, paving the way for the development of new materials, pharmaceuticals, and biologically active molecules.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H319
Precautionary Statements P305+P351+P338
Class N/A
Packing Group N/A

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