Cas no 211812-04-3 (tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate)

Tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate is a specialized carbamate derivative used in organic synthesis and pharmaceutical applications. Its key structural features include a tert-butyloxycarbonyl (Boc) protecting group and a hydroxyl-functionalized isobutyl moiety, offering versatility in peptide synthesis and intermediate preparation. The Boc group provides selective protection for amines, while the hydroxyl group enables further functionalization. This compound is valued for its stability under basic conditions and ease of deprotection under acidic conditions, making it suitable for controlled reaction sequences. Its well-defined reactivity profile ensures reproducibility in complex synthetic pathways, particularly in medicinal chemistry and drug development.
tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate structure
211812-04-3 structure
Product Name:tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate
CAS No:211812-04-3
MF:C9H19NO4
MW:205.25146317482
MDL:MFCD24466270
CID:1023493
PubChem ID:10845899
Update Time:2025-10-29

tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate Chemical and Physical Properties

Names and Identifiers

    • Carbamic acid, (2-hydroxy-1,1-dimethylethoxy)-, 1,1-dimethylethyl ester (9CI)
    • tert-butyl 1-hydroxy-2-methylpropan-2-yloxycarbamate
    • tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate
    • MDL: MFCD24466270
    • Inchi: 1S/C9H19NO4/c1-8(2,3)13-7(12)10-14-9(4,5)6-11/h11H,6H2,1-5H3,(H,10,12)
    • InChI Key: ZOGLEOIAQNHQHA-UHFFFAOYSA-N
    • SMILES: O(C(C)(C)CO)NC(=O)OC(C)(C)C

Computed Properties

  • Exact Mass: 205.13147

Experimental Properties

  • PSA: 67.79

tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
B140153-10mg
tert-butyl N-[(1-hydroxy-2-methylpropan-2-yl)oxy]carbamate
211812-04-3
10mg
$ 70.00 2022-06-07
TRC
B140153-50mg
tert-butyl N-[(1-hydroxy-2-methylpropan-2-yl)oxy]carbamate
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TRC
B140153-100mg
tert-butyl N-[(1-hydroxy-2-methylpropan-2-yl)oxy]carbamate
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$ 340.00 2022-06-07
Enamine
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tert-butyl N-[(1-hydroxy-2-methylpropan-2-yl)oxy]carbamate
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Enamine
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Enamine
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tert-butyl N-[(1-hydroxy-2-methylpropan-2-yl)oxy]carbamate
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Enamine
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tert-butyl N-[(1-hydroxy-2-methylpropan-2-yl)oxy]carbamate
211812-04-3 95%
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Enamine
EN300-227282-1.0g
tert-butyl N-[(1-hydroxy-2-methylpropan-2-yl)oxy]carbamate
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$528.0 2024-06-20
Enamine
EN300-227282-2.5g
tert-butyl N-[(1-hydroxy-2-methylpropan-2-yl)oxy]carbamate
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Additional information on tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate

Comprehensive Overview of tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate (CAS No. 211812-04-3)

In the realm of specialty chemicals, tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate (CAS No. 211812-04-3) has garnered significant attention due to its versatile applications in pharmaceuticals, agrochemicals, and material science. This compound, often referred to by its systematic name or abbreviated as tert-butyl carbamate derivative, is a key intermediate in synthetic chemistry. Its unique molecular structure, featuring a hydroxy group and a tert-butyl moiety, enables selective reactivity in complex reactions, making it invaluable for researchers and industrial chemists alike.

The synthesis of tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate involves multi-step organic transformations, often leveraging Boc-protection strategies (tert-butoxycarbonyl) to achieve high purity. Recent advancements in green chemistry have prompted interest in optimizing its production to reduce environmental impact—a topic frequently searched in AI-driven chemical research platforms. Users often inquire about scalable synthesis methods or alternative solvents for this compound, reflecting the industry's shift toward sustainability.

One of the most discussed applications of CAS No. 211812-04-3 is its role in peptide synthesis and drug discovery. As the pharmaceutical industry races to develop novel therapeutics, intermediates like this carbamate derivative are critical for constructing N-protected amino acids. Searches for "Boc-protecting group efficiency" or "carbamate stability in drug formulations" highlight its relevance in bioconjugation and prodrug design—topics trending in AI-curated literature databases.

Beyond pharmaceuticals, tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate finds utility in polymer chemistry, where its degradable carbamate linkage aligns with the demand for sustainable materials. Researchers exploring self-healing polymers or stimuli-responsive coatings frequently investigate this compound's compatibility with radical polymerization. Notably, forums on computational chemistry tools often feature discussions about predicting its thermodynamic properties using molecular modeling software.

From a regulatory standpoint, CAS No. 211812-04-3 is not classified as hazardous under major chemical inventories, which simplifies its global trade. However, quality control remains a priority, with HPLC purity analysis and spectroscopic characterization (e.g., NMR, IR) being common search queries among buyers. The compound's hygroscopic nature also prompts questions about storage conditions—a practical concern addressed in technical datasheets.

In conclusion, tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)oxycarbamate exemplifies how niche intermediates drive innovation across industries. Its intersection with green chemistry, AI-aided drug design, and advanced materials ensures its continued relevance in scientific discourse. For those seeking custom synthesis or structure-activity data, this compound offers a compelling case study in modern chemical R&D.

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