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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)-

1-ETHYL-5-METHYL-1H-PYRAZOLE-4-CARBALDEHYDE

Cc1c(C=O)cnn1CC Request for Quotation
Chemical Name: 1-ETHYL-5-METHYL-1H-PYRAZOLE-4-CARBALDEHYDE
CAS Number: 933778-29-1
Product Number: AG00GRS1(AGN-PC-0JT43Z)
Synonyms:
MDL No:
Molecular Formula: C7H10N2O
Molecular Weight: 138.1671

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
138.17g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
138.079g/mol
Monoisotopic Mass:
138.079g/mol
Topological Polar Surface Area:
34.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
127
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

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Chemical Structure


1-Ethyl-5-methyl-1H-pyrazole-4-carbaldehyde, also known as $name$, is a versatile chemical compound widely utilized in chemical synthesis. This compound plays a crucial role in the development of various synthetic processes due to its unique molecular structure and reactivity.One key application of 1-Ethyl-5-methyl-1H-pyrazole-4-carbaldehyde is as a key building block in the synthesis of heterocyclic compounds. Its presence in the chemical reaction can facilitate the formation of complex ring structures, making it a valuable tool in the creation of novel organic molecules.Furthermore, 1-Ethyl-5-methyl-1H-pyrazole-4-carbaldehyde can also serve as a precursor in the synthesis of pharmaceutical intermediates. By incorporating this compound into the synthesis pathway, chemists can efficiently access a variety of biologically active molecules with potential therapeutic applications.Overall, the versatile nature of 1-Ethyl-5-methyl-1H-pyrazole-4-carbaldehyde makes it a valuable asset in chemical synthesis, enabling the design and creation of innovative compounds with diverse functionalities.