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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-Ala-oall hcl

C[C@@H](C(=O)OCC=C)N.Cl Request for Quotation
Chemical Name: H-Ala-oall hcl
CAS Number: 203799-82-0
Product Number: AG00C3IX(AGN-PC-0WADEV)
Synonyms:
MDL No: MFCD01074682
Molecular Formula: C6H12ClNO2
Molecular Weight: 165.6180

Identification/Properties

Computed Properties
Molecular Weight:
165.617g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
165.056g/mol
Monoisotopic Mass:
165.056g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
112
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


H-ALA-OALL HCL is a crucial reagent in chemical synthesis, particularly in the field of peptide chemistry. Due to its unique properties, H-ALA-OALL HCL is commonly used in solid-phase peptide synthesis (SPPS) to facilitate the controlled and efficient assembly of peptides.When incorporated into the peptide chain, H-ALA-OALL HCL serves as a protected amino acid, allowing for stepwise elongation of the peptide sequence. Its compatibility with common coupling agents and activation methods makes it a versatile building block for the synthesis of peptide libraries, biologically active peptides, and peptide mimetics.Furthermore, H-ALA-OALL HCL exhibits excellent solubility in organic solvents commonly used in peptide synthesis, enabling convenient handling and manipulation during the synthetic process. Its stability under typical SPPS conditions ensures high yields and purity of the desired peptide product.In summary, the application of H-ALA-OALL HCL in chemical synthesis offers chemists a valuable tool for the efficient and reliable creation of diverse peptides with tailored sequences and functional properties.