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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)-

1,2-Propanediol, 3,3-diethoxy-

CCOC(C(CO)O)OCC Request for Quotation
Chemical Name: 1,2-Propanediol, 3,3-diethoxy-
CAS Number: 10487-05-5
Product Number: AG003PTV(AGN-PC-060HAL)
Synonyms:
MDL No:
Molecular Formula: C7H16O4
Molecular Weight: 164.19954

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
164.201g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
164.105g/mol
Monoisotopic Mass:
164.105g/mol
Topological Polar Surface Area:
58.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
80.5
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:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile compound with a wide range of applications in chemical synthesis. One notable use of 3,3-Diethoxypropane-1,2-diol is as a reagent for protecting hydroxyl groups in organic synthesis. By forming acetals with hydroxyl groups, this compound can shield them from unwanted reactions during various chemical transformations. This protective function is crucial in multi-step organic syntheses where selective reactions are desired, making 3,3-Diethoxypropane-1,2-diol a valuable tool for synthetic chemists. Additionally, this compound can also serve as a source of acetal-protected aldehydes and ketones, enabling controlled manipulation of functional groups in complex molecules. Its ease of use and compatibility with a variety of reaction conditions make 3,3-Diethoxypropane-1,2-diol a key component in the toolbox of synthetic chemists seeking to construct intricate molecular architectures.