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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)-

Furan, tetrahydro-3-methyl-

CC1COCC1 Request for Quotation
Chemical Name: Furan, tetrahydro-3-methyl-
CAS Number: 13423-15-9
Product Number: AG0033RN(AGN-PC-0JM2XA)
Synonyms:
MDL No:
Molecular Formula: C5H10O
Molecular Weight: 86.1323

Identification/Properties

Properties
MP:
-137°C (estimate)
BP:
83.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Refractive Index:
1.41979
Computed Properties
Molecular Weight:
86.134g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
86.073g/mol
Monoisotopic Mass:
86.073g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
43.2
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
2536
Hazard Statements:
H315-H319-H225
Precautionary Statements:
P501-P240-P210-P233-P243-P241-P242-P264-P280-P370+P378-P337+P313-P305+P351+P338-P362+P364-P303+P361+P353-P332+P313-P403+P235
Class:
3
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Methyltetrahydrofuran is a versatile solvent that finds widespread application in various chemical synthesis processes. Its unique properties make it an ideal choice for a range of reactions and procedures in the laboratory and industrial settings.Firstly, 3-Methyltetrahydrofuran is commonly used as a reaction solvent in organic synthesis due to its excellent solubilizing power and ability to dissolve a wide range of organic compounds. It is particularly useful in reactions involving sensitive compounds or those that are prone to side reactions, as it can provide a mild and inert reaction environment.Additionally, 3-Methyltetrahydrofuran is a preferred solvent for metal-catalyzed reactions, such as metal-catalyzed cross-coupling reactions and organometallic reactions. Its stability in the presence of reactive metal catalysts allows for efficient and high-yield transformations, making it an essential component in the toolbox of synthetic chemists working in these areas.Furthermore, 3-Methyltetrahydrofuran is utilized in various extraction and purification processes, thanks to its high selectivity and efficiency in separating target compounds from complex mixtures. Its low boiling point and good extraction capabilities make it a valuable solvent for processes like liquid-liquid extractions and crystallization techniques.Overall, the application of 3-Methyltetrahydrofuran in chemical synthesis spans a wide range of reactions and processes, making it an indispensable solvent for researchers and chemists working in the field of organic and inorganic chemistry.