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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)-

Benzenemethanol, 2,3,4-trimethoxy-

OCc1ccc(c(c1OC)OC)OC Request for Quotation
Chemical Name: Benzenemethanol, 2,3,4-trimethoxy-
CAS Number: 71989-96-3
Product Number: AG00328S(AGN-PC-0JLOJB)
Synonyms:
MDL No:
Molecular Formula: C10H14O4
Molecular Weight: 198.2158

Identification/Properties

Properties
BP:
310.9°C at 760 mmHg
Storage:
Room Temperature;Keep in dry area;
Form:
Liquid
Computed Properties
Molecular Weight:
198.218g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
198.089g/mol
Monoisotopic Mass:
198.089g/mol
Topological Polar Surface Area:
47.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
162
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2,3,4-Trimethoxyphenyl)methanol, also known as TMPM, serves a crucial role in chemical synthesis as a versatile building block. With its unique structure and reactivity, TMPM is commonly employed in the synthesis of various organic compounds. Its presence in the synthesis process adds functionality and complexity to the final products. As a key intermediate, TMPM facilitates the formation of diverse chemical structures, making it a valuable tool in the production of pharmaceuticals, agrochemicals, and materials. In organic synthesis, TMPM is utilized for constructing important chemical motifs and functional groups, enabling the creation of novel molecules with tailored properties and applications. Its strategic incorporation into reaction pathways enables efficient and selective transformations, leading to the synthesis of intricate molecules with high precision and control. In summary, (2,3,4-Trimethoxyphenyl)methanol plays a pivotal role in chemical synthesis, driving innovation and advancement in the field of organic chemistry.