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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)-

spiro[1,2-dihydroindole-3,4'-oxane]

O1CCC2(CC1)CNc1c2cccc1 Request for Quotation
Chemical Name: spiro[1,2-dihydroindole-3,4'-oxane]
CAS Number: 859164-46-8
Product Number: AG003FEY(AGN-PC-0COHS1)
Synonyms:
MDL No:
Molecular Formula: C12H15NO
Molecular Weight: 189.2536

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
189.258g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
189.115g/mol
Monoisotopic Mass:
189.115g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
210
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2',3',5',6'-Tetrahydrospiro[indoline-3,4'-pyran] plays a crucial role in chemical synthesis, particularly in the field of organic chemistry. Known for its unique structural properties, this molecule serves as a versatile building block in the creation of various organic compounds. Its spirocyclic structure offers a diverse range of reactivity, making it a valuable intermediate in the synthesis of complex molecules and pharmaceuticals. In chemical reactions, 2',3',5',6'-Tetrahydrospiro[indoline-3,4'-pyran] can undergo transformations such as cyclization, functional group modifications, and stereochemical control, allowing for the efficient construction of intricate molecular architectures. This compound's utility in chemical synthesis enables researchers to design and access new compounds with potential applications in drug discovery, material science, and other innovative fields.