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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)-

tert-butyl N-(1-benzhydrylazetidin-3-yl)carbamate

O=C(OC(C)(C)C)NC1CN(C1)C(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: tert-butyl N-(1-benzhydrylazetidin-3-yl)carbamate
CAS Number: 91189-18-3
Product Number: AG006Q70(AGN-PC-00NXDV)
Synonyms:
MDL No:
Molecular Formula: C21H26N2O2
Molecular Weight: 338.4433

Identification/Properties

Properties
BP:
448.8 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
338.451g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
338.199g/mol
Monoisotopic Mass:
338.199g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
410
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of 1,1-Dimethylethyl N-[1-(diphenylmethyl)-3-azetidinyl]carbamate in chemical synthesis lies in its utility as a versatile reagent for introducing the carbamate functional group into various organic molecules. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. By acting as a carbamoylating agent, it facilitates the modification of target molecules to impart desired properties or functionalities. Furthermore, its unique structural features enable specific interactions with target substrates, leading to selective transformations in complex synthetic pathways. Overall, 1,1-Dimethylethyl N-[1-(diphenylmethyl)-3-azetidinyl]carbamate plays a crucial role in the tailored design and construction of complex organic compounds through strategic chemical synthesis methods.