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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-Propanol, 1,3-dimethoxy-

COCC(COC)O Request for Quotation
Chemical Name: 2-Propanol, 1,3-dimethoxy-
CAS Number: 623-69-8
Product Number: AG003DK6(AGN-PC-0JKAGO)
Synonyms:
MDL No:
Molecular Formula: C5H12O3
Molecular Weight: 120.1470

Identification/Properties

Properties
BP:
169°C at N/A mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
1.4192
Computed Properties
Molecular Weight:
120.148g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
120.079g/mol
Monoisotopic Mass:
120.079g/mol
Topological Polar Surface Area:
38.7A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
40.9
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+H312+H332-H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,3-Dimethoxy-2-propanol, also known as DMP, serves as a versatile chemical reagent in various organic synthesis reactions. This compound is commonly utilized as a solvent, a reagent, or a precursor in the production of pharmaceuticals, agrochemicals, and fine chemicals. In chemical synthesis, 1,3-Dimethoxy-2-propanol can be employed as a protecting group reagent for aldehydes and ketones, enabling selective transformations during the synthesis of complex organic molecules. Additionally, DMP can act as a reagent for the preparation of various esters, ethers, and acetals due to its unique chemical properties. Its use in these reactions contributes to the efficient formation of specific chemical bonds and functional groups, making it an indispensable tool in the toolkit of synthetic chemists.