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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)-

(1R)-2-amino-1-pyridin-3-ylethanol

NCC(c1cccnc1)O Request for Quotation
Chemical Name: (1R)-2-amino-1-pyridin-3-ylethanol
CAS Number: 92990-44-8
Product Number: AG006JI0(AGN-PC-04564U)
Synonyms:
MDL No:
Molecular Formula: C7H10N2O
Molecular Weight: 138.1671

Identification/Properties

Properties
BP:
317.5 °C at 760 mmHg
Storage:
2-8℃;Light sensitive;
Computed Properties
Molecular Weight:
138.17g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
138.079g/mol
Monoisotopic Mass:
138.079g/mol
Topological Polar Surface Area:
59.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
97.6
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:
Danger
UN#:
2735
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-1-(pyridin-3-yl)ethanol, also known as $name$, is a versatile chemical compound widely used in chemical synthesis processes. Its unique molecular structure makes it a valuable building block in the creation of various compounds with pharmaceutical, agricultural, and materials science applications.In chemical synthesis, 2-Amino-1-(pyridin-3-yl)ethanol serves as a key intermediate for the production of diverse compounds due to its ability to participate in a range of reactions. It can undergo functional group transformations, such as acylation, alkylation, and condensation reactions, allowing for the modification of its chemical structure to tailor its properties for specific applications.Furthermore, 2-Amino-1-(pyridin-3-yl)ethanol plays a crucial role in the synthesis of bioactive molecules, pharmaceuticals, herbicides, and various functional materials. Its presence in the synthesis pathway can impart desired biological activities, enhance chemical stability, or improve material properties, depending on the intended application.Overall, the versatility and reactivity of 2-Amino-1-(pyridin-3-yl)ethanol make it a valuable component in the toolkit of synthetic chemists, enabling the efficient preparation of a wide range of compounds with diverse functionalities and applications.