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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)-

2-chloro-4-isopropylpyrimidine

Clc1nccc(n1)C(C)C Request for Quotation
Chemical Name: 2-chloro-4-isopropylpyrimidine
CAS Number: 941294-36-6
Product Number: AG005U85(AGN-PC-04TKV1)
Synonyms:
MDL No: MFCD09475913
Molecular Formula: C7H9ClN2
Molecular Weight: 156.6128

Identification/Properties

Properties
BP:
247.7 °C at 760 mmHg
Storage:
2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
156.613g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
156.045g/mol
Monoisotopic Mass:
156.045g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
106
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#:
2810
Hazard Statements:
H301
Precautionary Statements:
P264-P270-P301+P310+P330-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-4-isopropylpyrimidine is a versatile compound widely used in chemical synthesis for various applications. In organic chemistry, it serves as a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. The unique structure of this compound makes it an essential intermediate in the manufacturing of diverse chemical products. Its reactivity and compatibility with a range of functional groups make it an ideal candidate for use in complex chemical reactions. As a key component in the synthesis of biologically active compounds, 2-Chloro-4-isopropylpyrimidine plays a crucial role in the development of new materials with potential applications in the pharmaceutical and agricultural industries. Its versatile nature and wide array of uses make it a valuable tool for chemists and researchers seeking innovative solutions in chemical synthesis.