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  2. 2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid

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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-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid

O=C(NC(C(=O)O)NC(=O)OC(C)(C)C)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid
CAS Number: 176039-39-7
Product Number: AG00ADS1(AGN-PC-0KKKU1)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
412.442g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
412.163g/mol
Monoisotopic Mass:
412.163g/mol
Topological Polar Surface Area:
114A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
624
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:
H302-H312-H332
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (RS)-2-(BOC-AMINO)-2-(FMOC-AMINO)-ACETIC ACID is a versatile compound commonly used in chemical synthesis for the protection of amino groups. In organic synthesis, it serves as a key building block for the creation of peptides and peptide-like molecules.When incorporated into a synthesis strategy, the (RS)-2-(BOC-AMINO)-2-(FMOC-AMINO)-ACETIC ACID acts as a protecting group for the amino functionality. By selectively masking the amino group with the BOC and FMOC groups, chemists can control the reactivity of specific functional groups during various reaction steps. This protection-deprotection strategy allows for the desired transformations to occur at specific sites within the molecule, enabling the synthesis of complex peptide sequences with high precision.Furthermore, the (RS)-2-(BOC-AMINO)-2-(FMOC-AMINO)-ACETIC ACID offers compatibility with a wide range of coupling reagents and reaction conditions, making it a valuable tool in peptide chemistry. Its ability to facilitate the stepwise assembly of peptide chains enables the synthesis of custom peptides for use in drug discovery, biological research, and therapeutic applications.Overall, the (RS)-2-(BOC-AMINO)-2-(FMOC-AMINO)-ACETIC ACID plays a crucial role in the controlled and efficient synthesis of peptides, demonstrating its significance in the field of chemical synthesis.