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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Carbamic acid, (2-hydroxy-1-methylethyl)-, 1,1-dimethylethyl ester

OCC(NC(=O)OC(C)(C)C)C Request for Quotation
Chemical Name: Carbamic acid, (2-hydroxy-1-methylethyl)-, 1,1-dimethylethyl ester
CAS Number: 147252-84-4
Product Number: AG001EQS(AGN-PC-00LF6N)
Synonyms:
MDL No:
Molecular Formula: C8H17NO3
Molecular Weight: 175.2255

Identification/Properties

Properties
MP:
52-59 °C
BP:
276.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
175.228g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
175.121g/mol
Monoisotopic Mass:
175.121g/mol
Topological Polar Surface Area:
58.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
151
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tert-Butyl (1-hydroxypropan-2-yl)carbamate, also known as $name$, is a versatile compound commonly used in chemical synthesis. Its application in organic chemistry is particularly valuable due to its ability to act as a protective group for amines. By temporarily masking the amino group in a molecule with $name$, chemists can selectively manipulate other functional groups without affecting the amine functionality.In chemical synthesis, the use of $name$ as a protecting group allows for precise control over reactions involving amines. This protection strategy is crucial in multi-step synthesis processes where chemoselectivity is vital. By incorporating $name$ into a molecule, chemists can prevent unwanted reactivity or side reactions involving the amine group, thereby enabling the synthesis of complex molecules with high efficiency and selectivity.Moreover, the deprotection of the carbamate group can be easily achieved under specific conditions, providing a convenient way to reveal the original amine functionality in the molecule. This reversible process ensures that the desired product is obtained while maintaining the integrity of the amine group for further structural modifications or functional group interconversions.Overall, the strategic use of tert-Butyl (1-hydroxypropan-2-yl)carbamate in chemical synthesis offers chemists a powerful tool to enhance synthetic efficiency, increase selectivity, and expand the scope of organic transformations, making it a valuable asset in the toolbox of synthetic chemists.