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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)-

D-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-(triphenylmethyl)-

O=C(N[C@@H](C(=O)O)COC(c1ccccc1)(c1ccccc1)c1ccccc1)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: D-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-(triphenylmethyl)-
CAS Number: 212688-51-2
Product Number: AG00BERH(AGN-PC-0O7U0K)
Synonyms:
MDL No:
Molecular Formula: C37H31NO5
Molecular Weight: 569.6457

Identification/Properties

Computed Properties
Molecular Weight:
569.657g/mol
XLogP3:
7.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
11
Exact Mass:
569.22g/mol
Monoisotopic Mass:
569.22g/mol
Topological Polar Surface Area:
84.9A^2
Heavy Atom Count:
43
Formal Charge:
0
Complexity:
837
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound D-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-(triphenylmethyl) is a valuable reagent in chemical synthesis. It is commonly utilized as a chiral building block for the creation of complex organic molecules. Due to its specific structural properties, this compound plays a crucial role in the development of new pharmaceuticals, agrochemicals, and materials. By serving as a versatile intermediate, it enables chemists to efficiently construct stereochemically pure compounds with enhanced biological activity or desirable physical properties. The incorporation of D-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-O-(triphenylmethyl) in synthetic pathways empowers researchers to access a wide range of structurally diverse and functionally rich chemical entities, ultimately driving innovation in the field of organic chemistry.