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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-[2-(Cbz-amino)phenyl]-1,3-dioxolane

O=C(Nc1ccccc1C1OCCO1)OCc1ccccc1 Request for Quotation
Chemical Name: 2-[2-(Cbz-amino)phenyl]-1,3-dioxolane
CAS Number: 1346597-58-7
Product Number: AG003G8H(AGN-PC-0WA5WT)
Synonyms:
MDL No: MFCD20491415
Molecular Formula: C17H17NO4
Molecular Weight: 299.3212

Identification/Properties

Computed Properties
Molecular Weight:
299.32g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
299.115758g/mol
Monoisotopic Mass:
299.115758g/mol
Topological Polar Surface Area:
56.8Ų
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
351
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-[2-(Cbz-amino)phenyl]-1,3-dioxolane is a versatile compound commonly used in chemical synthesis as a valuable building block. This molecule is well-known for its significance in the creation of complex organic compounds due to its unique structural properties. It serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and materials.In organic synthesis, 2-[2-(Cbz-amino)phenyl]-1,3-dioxolane acts as a crucial starting material for the preparation of heterocyclic compounds and biologically active molecules. Its functional groups enable it to participate in a wide range of reactions, leading to the formation of diverse organic structures with specific properties. Additionally, the presence of the Cbz (carboxybenzyl) protecting group enhances the compound's stability and facilitates controlled transformations.Moreover, 2-[2-(Cbz-amino)phenyl]-1,3-dioxolane plays a significant role in the development of new synthetic methodologies and strategies in organic chemistry. Its reactivity and versatility make it a valuable tool for chemists seeking to construct complex molecular architectures efficiently. By incorporating this compound into their synthetic routes, researchers can access novel chemical entities and advance the field of organic synthesis.Overall, the application of 2-[2-(Cbz-amino)phenyl]-1,3-dioxolane in chemical synthesis underscores its importance as a fundamental building block with diverse synthetic capabilities. Its strategic use in the creation of intricate organic molecules highlights its relevance in advancing the frontier of synthesis and expanding the possibilities for designing new materials and substances.