1. Home
  2. D-Homoserine

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

D-Homoserine

OCC[C@H](C(=O)O)N Request for Quotation
Chemical Name: D-Homoserine
CAS Number: 6027-21-0
Product Number: AG0034P1(AGN-PC-0OD2QP)
Synonyms:
MDL No:
Molecular Formula: C4H9NO3
Molecular Weight: 119.1192

Identification/Properties

Properties
MP:
205 °C (dec.)(lit.)
BP:
368.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
8.0 ° (C=2, H2O)
Computed Properties
Molecular Weight:
119.12g/mol
XLogP3:
-4.4
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
119.058g/mol
Monoisotopic Mass:
119.058g/mol
Topological Polar Surface Area:
83.6A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
83.4
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


D-Homoserine is a versatile compound commonly utilized in chemical synthesis as a key building block for the preparation of various important chemicals and pharmaceuticals. Its application in organic chemistry is particularly significant due to its ability to serve as a precursor in the synthesis of various amino acids, peptides, and heterocyclic compounds. By incorporating D-Homoserine into chemical reactions, researchers can efficiently access a wide range of complex molecules, making it an essential component in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique chemical structure and reactivity make it a valuable tool for organic chemists seeking to create novel compounds and explore new avenues in chemical synthesis.