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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)-

Cyclododecane

C1CCCCCCCCCCC1 Request for Quotation
Chemical Name: Cyclododecane
CAS Number: 294-62-2
Product Number: AG002Y9Z(AGN-PC-0JK8YO)
Synonyms:
MDL No:
Molecular Formula: C12H24
Molecular Weight: 168.3190

Identification/Properties

Properties
MP:
59-61°C
BP:
247.0°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.4860 (estimate)
Computed Properties
Molecular Weight:
168.324g/mol
XLogP3:
6.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
168.188g/mol
Monoisotopic Mass:
168.188g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
43
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#:
3077
Hazard Statements:
H413
Precautionary Statements:
P273-P501
Class:
9
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Cyclododecane is a versatile compound widely used in chemical synthesis for its unique properties. Its main application lies in its ability to serve as a temporary protective coating for various materials and surfaces. In the realm of chemistry, Cyclododecane acts as a molecular "cage" that can encapsulate and protect sensitive compounds or substrates during reactions. This protective function is particularly valuable in the field of organic synthesis, where Cyclododecane can shield reactive functional groups from unwanted reactions or environmental factors.Furthermore, Cyclododecane can also act as a mold-release agent in the synthesis of intricate structures and complex molecules. By coating a substrate with Cyclododecane, chemists can facilitate the easy removal of the final product from the mold, ensuring the preservation of its intended shape and structure. This application is especially beneficial in the fabrication of specialized materials, such as resins, adhesives, and advanced polymers.Overall, the versatility and protective capabilities of Cyclododecane make it a valuable tool in chemical synthesis, enabling researchers to explore new synthetic pathways, enhance reaction efficiency, and achieve precise control over reaction outcomes. Its unique properties open up a world of possibilities for innovative research and development in various fields of chemistry.