1. Home
  2. Carbamic acid, (3-amino-2,2-dimethylpropyl)-, 1,1-dimethylethyl ester

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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, (3-amino-2,2-dimethylpropyl)-, 1,1-dimethylethyl ester

NCC(CNC(=O)OC(C)(C)C)(C)C Request for Quotation
Chemical Name: Carbamic acid, (3-amino-2,2-dimethylpropyl)-, 1,1-dimethylethyl ester
CAS Number: 292606-35-0
Product Number: AG002XUL(AGN-PC-0L5KYN)
Synonyms:
MDL No:
Molecular Formula: C10H22N2O2
Molecular Weight: 202.2939

Identification/Properties

Properties
MP:
74 °C
BP:
293.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
202.298g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
202.168g/mol
Monoisotopic Mass:
202.168g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
195
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The tert-Butyl (3-amino-2,2-dimethylpropyl)carbamate serves as a valuable reagent in chemical synthesis, specifically in organic chemistry applications. This compound is commonly utilized as a protecting group for amines during multi-step organic synthesis processes. By introducing the tert-butyl (3-amino-2,2-dimethylpropyl)carbamate onto amine functional groups, it can shield the amine from unwanted reactions or interactions with other reagents or functional groups. This protection allows chemists to selectively target other parts of the molecule for reactions, enabling precise control over the synthesis pathway. The tert-Butyl (3-amino-2,2-dimethylpropyl)carbamate's stability and ease of installation make it a versatile tool for manipulating amine-containing molecules in the laboratory.