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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)-

Isoindolin-5-ol hydrochloride

Oc1ccc2c(c1)CNC2.Cl Request for Quotation
Chemical Name: Isoindolin-5-ol hydrochloride
CAS Number: 1126832-40-3
Product Number: AG00HCF6(AGN-PC-0WR45P)
Synonyms:
MDL No: MFCD10700137
Molecular Formula: C8H10ClNO
Molecular Weight: 171.6241

Identification/Properties

Computed Properties
Molecular Weight:
171.624g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
171.045g/mol
Monoisotopic Mass:
171.045g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
126
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Isoindolin-5-ol hydrochloride, also known as 1,3-Dihydroisoindol-6-ol hydrochloride, is a versatile chemical building block widely used in the field of organic synthesis. Its unique structure and reactivity make it a valuable intermediate in the preparation of various organic compounds.Isoindolin-5-ol hydrochloride plays a crucial role in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. This compound can undergo a variety of chemical transformations, such as nucleophilic substitution, oxidation, and reduction reactions, to yield diverse products with different functionalities.In pharmaceutical chemistry, Isoindolin-5-ol hydrochloride is utilized in the development of new drug candidates and the modification of existing drugs. Its incorporation into drug molecules can enhance biological activity, improve pharmacokinetic properties, and increase the overall efficacy of the pharmaceutical compound.Furthermore, Isoindolin-5-ol hydrochloride is employed in the synthesis of organic dyes, pigments, and materials with specific optical properties. Its ability to participate in cyclization reactions and form stable aromatic structures makes it a valuable precursor for creating colorful and light-absorbing compounds.Overall, Isoindolin-5-ol hydrochloride serves as a versatile and indispensable reagent in chemical synthesis, offering chemists a wide range of possibilities for designing innovative molecules and materials. Its unique structural features and reactivity make it a valuable tool for researchers and synthetic chemists working in various fields of chemistry.