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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-Methylisoindolin-5-amine dihydrochloride

CN1Cc2c(C1)cc(cc2)N.Cl.Cl Request for Quotation
Chemical Name: 2-Methylisoindolin-5-amine dihydrochloride
CAS Number: 943751-30-2
Product Number: AG00IMOD(AGN-PC-0WAMBJ)
Synonyms:
MDL No:
Molecular Formula: C9H14Cl2N2
Molecular Weight: 221.1269

Identification/Properties

Computed Properties
Molecular Weight:
221.125g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
220.053g/mol
Monoisotopic Mass:
220.053g/mol
Topological Polar Surface Area:
29.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
147
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:
3
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


2-Methylisoindolin-5-amine dihydrochloride is a versatile compound widely used in chemical synthesis as a key building block in the creation of various organic molecules. As a primary amine, this compound can participate in diverse reactions such as condensation, nucleophilic substitution, and reductive amination, allowing for the synthesis of complex structures. Its unique structure also lends itself to the modification of aromatic systems, enabling the introduction of functional groups and stereoisomers with high selectivity. In addition, 2-Methylisoindolin-5-amine dihydrochloride can serve as a precursor for the preparation of pharmaceutical intermediates, agrochemicals, and materials for pharmaceutical research. Its utility in organic synthesis makes it a valuable tool for chemists seeking to design and develop novel compounds with tailored properties.