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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)-

2,3-dihydro-1H-indole-6-carboxylic acid;hydrochloride

OC(=O)c1ccc2c(c1)NCC2.Cl Request for Quotation
Chemical Name: 2,3-dihydro-1H-indole-6-carboxylic acid;hydrochloride
CAS Number: 15861-37-7
Product Number: AG001QCE(AGN-PC-09RR0Y)
Synonyms:
MDL No:
Molecular Formula: C9H10ClNO2
Molecular Weight: 199.6342

Identification/Properties

Computed Properties
Molecular Weight:
199.634g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
199.04g/mol
Monoisotopic Mass:
199.04g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
193
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Indoline-6-carboxylic acid hydrochloride is a versatile chemical compound widely used in chemical synthesis. This compound serves as a key building block in the development of pharmaceuticals, agrochemicals, and various organic compounds.In chemical synthesis, Indoline-6-carboxylic acid hydrochloride acts as a valuable intermediate for the synthesis of indole-based compounds. Its functional groups and structural properties make it a crucial component in the construction of complex molecules with diverse applications.Specifically, in pharmaceutical synthesis, this compound is utilized for the production of indole-containing drugs that exhibit promising biological activities. Its ease of functionalization allows for the modification of its structure to optimize desired pharmacological properties. Additionally, in agrochemical research, Indoline-6-carboxylic acid hydrochloride is employed for the synthesis of pesticides and herbicides with enhanced efficacy and reduced environmental impact.Overall, the application of Indoline-6-carboxylic acid hydrochloride in chemical synthesis facilitates the development of innovative compounds with potential therapeutic, agricultural, and industrial benefits.