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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)-

methyl 2,3-dihydro-1H-isoindole-5-carboxylate;hydrochloride

COC(=O)c1ccc2c(c1)CNC2.Cl Request for Quotation
Chemical Name: methyl 2,3-dihydro-1H-isoindole-5-carboxylate;hydrochloride
CAS Number: 127168-93-8
Product Number: AG000WQ4(AGN-PC-02KO45)
Synonyms:
MDL No:
Molecular Formula: C10H12ClNO2
Molecular Weight: 213.6608

Identification/Properties

Computed Properties
Molecular Weight:
213.661g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
213.056g/mol
Monoisotopic Mass:
213.056g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
205
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl isoindoline-5-carboxylate hydrochloride is a versatile compound used in chemical synthesis for various applications. This compound serves as a valuable building block in the creation of organic molecules, particularly in the pharmaceutical industry. Its unique structure and reactivity make it an important intermediate in the synthesis of biologically active compounds and drug candidates. By incorporating Methyl isoindoline-5-carboxylate hydrochloride into synthesis routes, chemists can efficiently access complex molecular scaffolds that are essential for drug discovery and development. Its ability to participate in a wide range of chemical reactions allows for the efficient modification and functionalization of molecules, enabling the synthesis of diverse chemical libraries for screening purposes. In addition, Methyl isoindoline-5-carboxylate hydrochloride's compatibility with various reaction conditions and its well-defined reactivity profile make it a valuable tool for organic chemists seeking to streamline synthetic routes and increase overall efficiency in the preparation of target molecules. Through its strategic incorporation into synthetic pathways, this compound plays a crucial role in the discovery and development of novel pharmaceutical agents and biologically active compounds.