1. Home
  2. 1H-Pyrazole-1-ethanol, 5-amino-3-methyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

1H-Pyrazole-1-ethanol, 5-amino-3-methyl-

Cc1cc(n(n1)CCO)N Request for Quotation
Chemical Name: 1H-Pyrazole-1-ethanol, 5-amino-3-methyl-
CAS Number: 51546-08-8
Product Number: AG00DCUZ(AGN-PC-0LL75Q)
Synonyms:
MDL No:
Molecular Formula: C6H11N3O
Molecular Weight: 141.1710

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
141.174g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
141.09g/mol
Monoisotopic Mass:
141.09g/mol
Topological Polar Surface Area:
64.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
109
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
1759
Hazard Statements:
H302-H315-H318-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P330-P332+P313-P362-P403+P233-P405-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-(5-Amino-3-methyl-1H-pyrazol-1-yl)ethanol is a versatile compound widely utilized in chemical synthesis as a key building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Known for its unique structure and functional properties, this compound plays a crucial role in the development of new organic molecules with diverse applications.In chemical synthesis, 2-(5-Amino-3-methyl-1H-pyrazol-1-yl)ethanol acts as a valuable intermediate in the production of biologically active compounds. Its functional groups enable a wide range of reactions, facilitating the attachment of different substituents to create complex molecular structures. This compound serves as a key component in the creation of novel drug candidates, agrochemicals with enhanced activity, and functional materials with specific properties.By incorporating 2-(5-Amino-3-methyl-1H-pyrazol-1-yl)ethanol into synthetic pathways, chemists can access a diverse array of molecules that exhibit desired biological, agricultural, or industrial properties. Its versatility and reactivity make it a valuable tool for designing and synthesizing advanced chemical compounds with tailored functions, paving the way for innovation and discovery in the field of organic chemistry.