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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)-

2,3,5-trimethylphenol

Cc1cc(C)c(c(c1)O)C Request for Quotation
Chemical Name: 2,3,5-trimethylphenol
CAS Number: 697-82-5
Product Number: AG005U0Q(AGN-PC-0JKARW)
Synonyms:
MDL No:
Molecular Formula: C9H12O
Molecular Weight: 136.1910

Identification/Properties

Properties
MP:
92-95 °C
BP:
231.1 °C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
136.194g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
136.089g/mol
Monoisotopic Mass:
136.089g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
111
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#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3,5-Trimethylphenol, also known as Toluene-2,4-dimethylphenol, is a versatile compound widely used in chemical synthesis processes. This compound plays a crucial role in various industrial applications due to its unique properties and reactivity.In chemical synthesis, 2,3,5-Trimethylphenol is commonly utilized as a precursor in the synthesis of specialty chemicals, such as antioxidants, pharmaceuticals, and fragrances. Its functionality as a phenol derivative allows for the introduction of specific functional groups through various chemical reactions, making it a valuable building block in organic synthesis.One of the key applications of 2,3,5-Trimethylphenol is its use as a starting material in the production of antioxidants, which are additives that inhibit the oxidation of other molecules. By incorporating 2,3,5-Trimethylphenol into antioxidant formulations, the stability and lifespan of various products can be significantly enhanced.Furthermore, 2,3,5-Trimethylphenol is also employed in the synthesis of pharmaceutical compounds, where its structural features can be modified to impart desired biological activities. Its presence in pharmaceutical intermediates allows for the creation of diverse drug substances with tailored properties and functionalities.Additionally, the use of 2,3,5-Trimethylphenol in fragrance synthesis is notable, as it contributes to the development of unique aroma compounds. By incorporating this compound into fragrance formulations, perfumers can create complex and captivating scents that appeal to different sensory preferences.Overall, the application of 2,3,5-Trimethylphenol in chemical synthesis underscores its importance as a versatile building block with significant implications across various industries.