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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)-

H-Lys(crotonyl)-OH

C/C=C/C(=O)NCCCC[C@@H](C(=O)O)N Request for Quotation
Chemical Name: H-Lys(crotonyl)-OH
CAS Number: 1338823-35-0
Product Number: AG009DJP(AGN-PC-0WCY1V)
Synonyms:
MDL No: MFCD22381072
Molecular Formula: C10H18N2O3
Molecular Weight: 214.2615

Identification/Properties

Computed Properties
Molecular Weight:
214.265g/mol
XLogP3:
-2.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
214.132g/mol
Monoisotopic Mass:
214.132g/mol
Topological Polar Surface Area:
92.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
239
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


H-Lys(crotonyl)-OH, also known as Nε-crotonyl-L-lysine, is a modified form of the amino acid lysine with a crotonyl group attached to the ε-amino group. This modified amino acid plays a significant role in chemical synthesis, particularly in the field of peptide chemistry.In chemical synthesis, H-Lys(crotonyl)-OH is often used as a building block for the creation of peptides with specific properties and functionalities. By incorporating this modified amino acid into peptide chains, researchers can tailor the structure and characteristics of peptides for various applications.One of the key advantages of using H-Lys(crotonyl)-OH in chemical synthesis is its ability to introduce structural diversity and chemical versatility into peptides. The crotonyl group can interact with other functional groups in the peptide chain, leading to changes in conformation and stability. This can be crucial for designing peptides with desired biological activities or improved properties for drug delivery systems.Additionally, H-Lys(crotonyl)-OH can serve as a valuable tool in studying protein structures and functions, as its introduction into peptides can mimic post-translational modifications that occur naturally in proteins. This can provide insights into the role of specific modifications in protein interactions, enzymatic activity, and cellular signaling pathways.Overall, the application of H-Lys(crotonyl)-OH in chemical synthesis offers a versatile approach to designing and studying peptides with tailored properties, making it a valuable component in peptide chemistry research.