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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-Acetamido-3-hydroxypropanoic acid

OCC(C(=O)O)NC(=O)C Request for Quotation
Chemical Name: 2-Acetamido-3-hydroxypropanoic acid
CAS Number: 97-14-3
Product Number: AG006NQU(AGN-PC-0WALXI)
Synonyms:
MDL No:
Molecular Formula: C5H9NO4
Molecular Weight: 147.1293

Identification/Properties

Properties
BP:
468.4±40.0°C at 760 mmHg
Storage:
Keep in dry area;-10 ℃;
Computed Properties
Molecular Weight:
147.13g/mol
XLogP3:
-1.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
147.053g/mol
Monoisotopic Mass:
147.053g/mol
Topological Polar Surface Area:
86.6A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
145
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2-Acetamido-3-hydroxypropanoic acid, also known as serine, plays a crucial role in chemical synthesis as a key building block in the production of various compounds. This versatile compound is commonly used in the pharmaceutical industry to synthesize pharmaceutical intermediates and drug molecules. Additionally, it is utilized in the development of peptide-based drugs and in the creation of chiral compounds due to its ability to act as a chiral auxiliary. Moreover, serine is employed in the food industry to produce amino acid supplements and flavor enhancers. In the field of biotechnology, this compound serves as a substrate for the enzymatic production of various amino acids. Its unique chemical properties make it an essential component in the synthesis of a wide range of valuable products across different industries.