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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)-

3-(Boc-aminomethyl)indoline

O=C(OC(C)(C)C)NCC1CNc2c1cccc2 Request for Quotation
Chemical Name: 3-(Boc-aminomethyl)indoline
CAS Number: 1000932-73-9
Product Number: AG0000W9(AGN-PC-0WA7JS)
Synonyms:
MDL No: MFCD09971405
Molecular Formula: C14H20N2O2
Molecular Weight: 248.3208

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
248.326g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
248.152g/mol
Monoisotopic Mass:
248.152g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
299
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Boc-aminomethyl)indoline, a versatile building block in chemical synthesis, is widely utilized in the development of various pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it valuable for the construction of complex organic molecules. One of the key applications of 3-(Boc-aminomethyl)indoline is in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. Additionally, it serves as a crucial intermediate in the preparation of chiral ligands and catalysts, enabling the efficient production of enantiopure compounds. Furthermore, this compound can be employed in the design and fabrication of novel organic materials with tailored properties, offering opportunities for advanced material science research and innovation. Through its strategic incorporation into synthetic pathways, 3-(Boc-aminomethyl)indoline plays a pivotal role in the advancement of diverse fields within the realm of chemistry.