1. Home
  2. 1-Imidazolidinecarboxylic acid, 1,1-dimethylethyl ester

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

1-Imidazolidinecarboxylic acid, 1,1-dimethylethyl ester

O=C(N1CNCC1)OC(C)(C)C Request for Quotation
Chemical Name: 1-Imidazolidinecarboxylic acid, 1,1-dimethylethyl ester
CAS Number: 916891-97-9
Product Number: AG003A8A(AGN-PC-0BT1GF)
Synonyms:
MDL No:
Molecular Formula: C8H16N2O2
Molecular Weight: 172.2248

Identification/Properties

Computed Properties
Molecular Weight:
172.228g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
172.121g/mol
Monoisotopic Mass:
172.121g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
174
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#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Tert-Butyl imidazolidine-1-carboxylate is a versatile chemical compound widely utilized in chemical synthesis processes. In the realm of organic chemistry, this compound plays a crucial role as a valuable protecting group for various functional groups. With its unique structure and reactivity, tert-Butyl imidazolidine-1-carboxylate acts as a protecting agent by shielding specific functional groups from unwanted reactions during synthetic procedures. This protection allows chemists to selectively manipulate and modify target molecules, enabling the synthesis of complex organic compounds with improved yields and purity. Additionally, tert-Butyl imidazolidine-1-carboxylate is known for its compatibility with a wide range of common reagents and reaction conditions, making it a go-to choice for chemists in need of reliable protection strategies in complex chemical syntheses.