1. Home
  2. H-D-Thr(bzl)-oh

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-D-Thr(bzl)-oh

C[C@@H]([C@H](C(=O)O)N)OCc1ccccc1 Request for Quotation
Chemical Name: H-D-Thr(bzl)-oh
CAS Number: 86062-17-1
Product Number: AG00GTUQ(AGN-PC-0WADF7)
Synonyms:
MDL No:
Molecular Formula: C11H15NO3
Molecular Weight: 209.2417

Identification/Properties

Computed Properties
Molecular Weight:
209.245g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
209.105g/mol
Monoisotopic Mass:
209.105g/mol
Topological Polar Surface Area:
72.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
202
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


H-D-THR(BZL)-OH is a key building block in chemical synthesis commonly used in peptide synthesis and drug development. This compound serves as a protected form of threonine, an essential amino acid, that allows for selective modification and manipulation of peptide chains. With its benzyl ester protecting group, H-D-THR(BZL)-OH offers stability during various synthetic reactions while enabling precise control over the addition of other amino acids or functional groups. Its versatile nature makes it an indispensable tool for chemists and researchers working on the synthesis of complex peptides and pharmaceutical compounds.