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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)-

2,5,8,11,14-Pentaoxahexadecan-16-ol

COCCOCCOCCOCCOCCO Request for Quotation
Chemical Name: 2,5,8,11,14-Pentaoxahexadecan-16-ol
CAS Number: 23778-52-1
Product Number: AG0035VO(AGN-PC-0JLYJ8)
Synonyms:
MDL No:
Molecular Formula: C11H24O6
Molecular Weight: 252.3047

Identification/Properties

Properties
BP:
332.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Refractive Index:
1.4480 to 1.4520
Computed Properties
Molecular Weight:
252.307g/mol
XLogP3:
-1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
14
Exact Mass:
252.157g/mol
Monoisotopic Mass:
252.157g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
133
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Pentaethylene glycol monomethyl ether, also known as PEM, is a versatile compound widely used in chemical synthesis applications. With its unique properties, PEM serves as an excellent solvent in various reactions, allowing for efficient mixing of reactants and products.In chemical synthesis, PEM can act as a reaction medium for catalytic processes, facilitating the dissolution and interaction of different components. Its solubility characteristics make it a suitable choice for reactions requiring a non-polar solvent, aiding in the formation of homogeneous mixtures.Furthermore, PEM can be utilized as a stabilizing agent in organic reactions, helping to control the rate of the reaction and enhance the selectivity of the desired products. Its compatibility with a wide range of organic compounds makes it a valuable tool in fine chemical synthesis.Overall, Pentaethylene glycol monomethyl ether plays a crucial role in chemical synthesis by providing a stable and efficient medium for various reactions, ultimately contributing to the successful formation of desired products.