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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)-

3-(4-bromopyrazol-1-yl)propan-1-ol

OCCCn1cc(cn1)Br Request for Quotation
Chemical Name: 3-(4-bromopyrazol-1-yl)propan-1-ol
CAS Number: 925180-06-9
Product Number: AG003KUK(AGN-PC-013P02)
Synonyms:
MDL No: MFCD06804869
Molecular Formula: C6H9BrN2O
Molecular Weight: 205.0525

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
205.055g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
203.99g/mol
Monoisotopic Mass:
203.99g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
102
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:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-1-(3-hydroxypropyl)pyrazole is a valuable chemical compound widely used in chemical synthesis processes. Its primary application lies in organic chemistry reactions where it serves as a versatile building block for the preparation of various pharmaceuticals, agrochemicals, and functional materials. With its unique structural properties, 4-Bromo-1-(3-hydroxypropyl)pyrazole can participate in a range of reactions such as substitution, addition, and condensation reactions, making it a crucial intermediate in the synthesis of complex organic molecules. This compound's strategic placement of the bromine and hydroxypropyl groups allows for selective functionalization, enabling chemists to modify its structure further to create novel compounds with desired properties. Overall, 4-Bromo-1-(3-hydroxypropyl)pyrazole plays a pivotal role in the field of chemical synthesis, facilitating the development of new compounds with potential applications in various industries.