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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[2H-1-benzopyran-2,2'-[2H]indole],6-bromo-1',3'-dihydro-1',3',3'-trimethyl-

Brc1ccc2c(c1)C=CC1(O2)N(C)c2c(C1(C)C)cccc2 Request for Quotation
Chemical Name: Spiro[2H-1-benzopyran-2,2'-[2H]indole],6-bromo-1',3'-dihydro-1',3',3'-trimethyl-
CAS Number: 16650-14-9
Product Number: AG001WSR(AGN-PC-0Q8X4N)
Synonyms:
MDL No:
Molecular Formula: C19H18BrNO
Molecular Weight: 356.2563

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
356.263g/mol
XLogP3:
5.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
355.057g/mol
Monoisotopic Mass:
355.057g/mol
Topological Polar Surface Area:
12.5A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
476
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


6-Bromo-1',3',3'-trimethylspiro[chromene-2,2'-indoline] is a versatile compound widely used in chemical synthesis processes. This compound serves as a valuable building block in the creation of various organic molecules and complex structures. Due to its unique molecular structure, 6-Bromo-1',3',3'-trimethylspiro[chromene-2,2'-indoline] exhibits reactivity that allows for selective functionalization at specific positions within the molecule. This special reactivity makes it a preferred reagent in the synthesis of pharmaceutical intermediates, agrochemicals, and advanced materials. Additionally, the spirocyclic nature of this compound imparts desirable stereochemical properties to the products formed during chemical transformations, making it particularly useful in the production of chiral compounds with high enantiomeric purity. Its application extends to the development of novel organic compounds with tailored properties for various industrial and research applications.