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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)-

(R)-Benzyl tert-butyl (3-hydroxypropane-1,2-diyl)dicarbamate

OC[C@H](NC(=O)OC(C)(C)C)CNC(=O)OCc1ccccc1 Request for Quotation
Chemical Name: (R)-Benzyl tert-butyl (3-hydroxypropane-1,2-diyl)dicarbamate
CAS Number: 1263045-28-8
Product Number: AG000SI5(AGN-PC-0WAMGJ)
Synonyms:
MDL No: MFCD06798156
Molecular Formula: C16H24N2O5
Molecular Weight: 324.3722

Identification/Properties

Computed Properties
Molecular Weight:
324.377g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
9
Exact Mass:
324.169g/mol
Monoisotopic Mass:
324.169g/mol
Topological Polar Surface Area:
96.9A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
375
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-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-Benzyl tert-butyl (3-hydroxypropane-1,2-diyl)dicarbamate compound serves as a versatile and valuable reagent in chemical synthesis processes. Its unique structure and functional groups enable it to participate in a variety of reactions, making it an essential component in organic chemistry transformations. This compound is particularly useful in asymmetric synthesis strategies, where the chirality of the benzyl and tert-butyl groups can be leveraged to control the stereochemistry of the final product. Additionally, its hydroxypropane backbone provides flexibility and additional functionalization opportunities, allowing for the construction of complex molecular architectures. In summary, (R)-Benzyl tert-butyl (3-hydroxypropane-1,2-diyl)dicarbamate is a vital tool for chemists seeking to design and synthesize intricate organic molecules with precision and efficiency.