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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)-

1,3-Propanediol, 2,2-dimethoxy-

OCC(CO)(OC)OC Request for Quotation
Chemical Name: 1,3-Propanediol, 2,2-dimethoxy-
CAS Number: 153214-82-5
Product Number: AG00AB6L(AGN-PC-0NGBFL)
Synonyms:
MDL No:
Molecular Formula: C5H12O4
Molecular Weight: 136.1464

Identification/Properties

Computed Properties
Molecular Weight:
136.147g/mol
XLogP3:
-1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
136.074g/mol
Monoisotopic Mass:
136.074g/mol
Topological Polar Surface Area:
58.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
63.4
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,2-Dimethoxypropane-1,3-diol, also known as DMPD, plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly used as a dual protecting group for sensitive functional groups in organic synthesis, particularly in the preparation of complex molecules such as pharmaceuticals and natural products.DMPD acts as a protective agent for alcohols, phenols, and amines during various synthetic reactions. By temporarily blocking these reactive sites, DMPD enables selective transformations to occur at other sites within the molecule. This protection-deprotection strategy helps chemists to control the sequence of reactions and prevent unwanted side reactions, ultimately facilitating the synthesis of structurally intricate compounds.Moreover, the use of DMPD in chemical synthesis offers advantages such as high efficiency, mild reaction conditions, and ease of handling. Its compatibility with a wide range of functional groups makes it a valuable tool in the toolbox of synthetic chemists seeking to construct complex molecules with precision and efficiency.