1. Home
  2. Pyrimidine, 2-chloro-4-methyl-5-nitro-

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)-

Pyrimidine, 2-chloro-4-methyl-5-nitro-

Clc1ncc(c(n1)C)[N+](=O)[O-] Request for Quotation
Chemical Name: Pyrimidine, 2-chloro-4-methyl-5-nitro-
CAS Number: 97821-70-0
Product Number: AG00IJZM(AGN-PC-01WH5W)
Synonyms:
MDL No:
Molecular Formula: C5H4ClN3O2
Molecular Weight: 173.5572

Identification/Properties

Computed Properties
Molecular Weight:
173.556g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
172.999g/mol
Monoisotopic Mass:
172.999g/mol
Topological Polar Surface Area:
71.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
160
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

Customer Feedback

Chemical Structure


2-Chloro-4-methyl-5-nitropyrimidine, a versatile chemical compound, finds widespread application in various chemical synthesis processes due to its unique properties. This compound serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and other fine chemicals. With its carefully designed structure, 2-Chloro-4-methyl-5-nitropyrimidine plays a crucial role as a key intermediate in the synthesis of complex organic molecules. Its reactivity allows for efficient functional group transformations, enabling chemists to access a diverse range of target compounds. Additionally, this compound's compatibility with a variety of reaction conditions makes it a valuable tool for organic chemists seeking to streamline synthetic pathways and improve overall efficiency in their research and development projects.