29908-11-0 Usage
Description
1,4-DIOXANE, 2-(HYDROXYMETHYL)-, also known as 2-Methanol-1,4-dioxane, is a heterocyclic organic compound derived from 1,4-Dioxane. It is characterized by the presence of a hydroxymethyl group attached to the dioxane ring, which provides it with unique chemical properties and reactivity. 1,4-DIOXANE, 2-(HYDROXYMETHYL)is utilized in various practical applications and is also commonly found in laboratory settings due to its versatility and stability.
Uses
Used in Chemical Synthesis:
1,4-DIOXANE, 2-(HYDROXYMETHYL)is used as a synthetic intermediate for the production of various chemicals and pharmaceuticals. Its hydroxymethyl group allows for further functionalization and modification, making it a valuable building block in the synthesis of complex molecules.
Used in Solvent Applications:
In the chemical industry, 1,4-DIOXANE, 2-(HYDROXYMETHYL)is used as a solvent for a wide range of substances. Its ability to dissolve both polar and nonpolar compounds makes it a versatile choice for various chemical processes and reactions.
Used in Laboratory Research:
Due to its stability and reactivity, 1,4-DIOXANE, 2-(HYDROXYMETHYL)is often employed in laboratory research as a reactant or a solvent. It is particularly useful in the synthesis of new compounds and the study of chemical reactions.
Used in the Pharmaceutical Industry:
1,4-DIOXANE, 2-(HYDROXYMETHYL)is used as a key component in the development of new drugs and pharmaceuticals. Its unique structure and properties make it an attractive candidate for the design of novel therapeutic agents.
Used in the Production of Polymers:
In the polymer industry, 1,4-DIOXANE, 2-(HYDROXYMETHYL)is used as a monomer in the synthesis of various types of polymers. Its ability to form covalent bonds with other monomers allows for the creation of polymers with specific properties and applications.
Used in the Cosmetics Industry:
1,4-DIOXANE, 2-(HYDROXYMETHYL)is also utilized in the cosmetics industry, where it serves as a component in the formulation of various personal care products. Its compatibility with a wide range of ingredients makes it a valuable addition to cosmetic formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 29908-11-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,0 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29908-11:
(7*2)+(6*9)+(5*9)+(4*0)+(3*8)+(2*1)+(1*1)=140
140 % 10 = 0
So 29908-11-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O3/c6-3-5-4-7-1-2-8-5/h5-6H,1-4H2
29908-11-0Relevant articles and documents
Meso-Tetra(dioxanyl)porphyrins: Neutral, low molecular weight, and chiral porphyrins with solubility in aqueous solutions
Brückner, Christian,Damunupola, DInusha,Jiang, Xu-Liang
, p. 734 - 740 (2021/07/02)
The synthesis of the low-molecular weight, meso-Tetra(dioxan-2-yl)porphyrin with considerable solubility in aqueous solution is described. The key intermediate dioxan-2-carbaldehyde is accessible in either racemic or in stereo-pure forms from commercially available starting materials in three steps. Using 4 × 1 or 2 + 2-Type syntheses provide the porphyrin in modest yields. While the racemic aldehyde created an intractable mixture of diastereomers, the enantiopure aldehyde created a single enantiomer of the target porphyrin. The porphyrin was spectroscopically characterized. As its free base or zinc complex, it showed excellent solubility properties in organic and aqueous solvents, though free water-solubility was not achieved. The work expands on the availability of chiral porphyrins and neutral porphyrins with considerable solubility in aqueous solution.
2-Hydroxymethyl-1,4-dioxane: Synthesis, resolution and determination of the absolute configurations of the enantiomers
Pallavicini, Marco,Valoti, Ermanno,Villa, Luigi
, p. 267 - 273 (2007/10/03)
2-Hydroxymethyl-1, 4-dioxane 3 was resolved via salt formation between its hydrogen phthalate and (R)- or (S)-1-phenylethylamine, selective crystallization of the resultant diastereomeric mixtures and subsequent recovery of its enantiomers by saponification. The progress of the resolution was followed by chiral HPLC and the absolute stereochemistry of the two enantiomers determined by comparison of their specific rotations with that of (R)-3 synthesized from enantiomerically pure (R)-1-O-benzylglycerol. The results of the synthesis of 3 and of its resolution are discussed and compared with those previously obtained for 1,2-isopropylidene glycerol evaluating the consequences of replacement of ispropylidene with an ethylene bridge.
Alkylation of active methylene compounds with 2-chloromethyl-1,4-dioxane
Krasavtsev I. I.,Basalkevich E. D.,Lozinskii M. O.
, p. 1632 - 1634 (2007/10/02)
The alkylation of some active methylene compounds with 2-chloromethyl-1,4-dioxane was investigated.It was shown that malonic ester gives mono- and dialkylation products, depending on the conditions.The alkylation of acetoacetic ester gives a mixture of C- and O-alkylation products.Acetylacetone is not alkylated under the given conditions but condenses fully, being converted into 2,4-dimethyl-6-hydroxyacetophenone.
