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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)-

2-Propanamine, N-(ethylcarbonimidoyl)-2-methyl-

CCC(=N)NC(C)(C)C Request for Quotation
Chemical Name: 2-Propanamine, N-(ethylcarbonimidoyl)-2-methyl-
CAS Number: 1433-27-8
Product Number: AG003ENP(AGN-PC-0O2MG9)
Synonyms:
MDL No:
Molecular Formula: C7H16N2
Molecular Weight: 128.21534

Identification/Properties

Computed Properties
Molecular Weight:
126.203g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
126.116g/mol
Monoisotopic Mass:
126.116g/mol
Topological Polar Surface Area:
24.7A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
124
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:
No

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-tert-Butyl-3-ethylcarbodiimide is a valuable reagent in chemical synthesis, particularly in peptide synthesis and drug development. This compound serves as a coupling reagent for the efficient formation of amide bonds between amino acids during peptide assembly. By facilitating peptide bond formation, 1-tert-Butyl-3-ethylcarbodiimide plays a crucial role in the production of peptides with specific sequences and structures, which are essential in various bioactive compounds like pharmaceutical drugs and peptides for research purposes. Additionally, this reagent is known for its high efficiency in promoting peptide bond formation while minimizing side reactions, making it a preferred choice in peptide chemistry. The application of 1-tert-Butyl-3-ethylcarbodiimide in chemical synthesis is a fundamental tool for researchers and chemists working in the field of peptide synthesis and drug discovery.