15833-61-1 Usage
Description
TETRAHYDRO-3-FURANMETHANOL, also known as THFM, is a colorless viscous liquid that is primarily formed during the hydrolysis of 1,3-dioxolane compounds. It is an organic compound with a unique structure that consists of a tetrahydrofuran ring and a hydroxymethyl group. Due to its chemical properties and structure, THFM has potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
TETRAHYDRO-3-FURANMETHANOL is used as an intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a versatile building block in the development of new drugs, particularly those targeting specific biological pathways.
Used in Chemical Synthesis:
TETRAHYDRO-3-FURANMETHANOL is used as a key intermediate in the synthesis of various organic compounds, including specialty chemicals, agrochemicals, and other fine chemicals. Its ability to form a tetrahydrofuran ring makes it a valuable component in the creation of complex molecular structures.
Used in Polymer Industry:
TETRAHYDRO-3-FURANMETHANOL is used as a monomer for the production of polymers with specific properties. The incorporation of THFM into polymer chains can result in materials with enhanced characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.
Used in Cosmetics Industry:
TETRAHYDRO-3-FURANMETHANOL is used as a component in the formulation of cosmetics and personal care products. Its compatibility with various ingredients and ability to improve the texture and consistency of formulations make it a valuable addition to the cosmetics industry.
Used in Flavor and Fragrance Industry:
TETRAHYDRO-3-FURANMETHANOL is used as a building block for the creation of unique fragrances and flavors. Its ability to contribute to the overall sensory profile of a product makes it an important component in the development of novel scents and tastes.
Check Digit Verification of cas no
The CAS Registry Mumber 15833-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,3 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15833-61:
(7*1)+(6*5)+(5*8)+(4*3)+(3*3)+(2*6)+(1*1)=111
111 % 10 = 1
So 15833-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O2/c6-3-5-1-2-7-4-5/h5-6H,1-4H2
15833-61-1Relevant articles and documents
3-(5-METHOXY-1-OXOISOINDOLIN-2-YL)PIPERIDINE-2,6-DIONE DERIVATIVES AND USES THEREOF
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Page/Page column 328-329, (2021/06/26)
The present disclosure relates to compounds of formula (I') and pharmaceutical compositions and their use in reducing Widely Interspaced Zinc Finger Motifs (WIZ) expression levels, or inducing fetal hemoglobin (HbF) expression, and in the treatment of inherited blood disorders (e.g., hemoglobinopathies, e.g., beta-hemoglobinopathies), such as sickle cell disease and beta-thalassemia.
Production technology for 3-hydroxymethyltetrahydrofuran
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Paragraph 0033; 0034; 0037; 0043, (2018/10/19)
The invention discloses a production technology for 3-hydroxymethyltetrahydrofuran, and belongs to the field of pesticide intermediate synthetic processes. The production technology is capable of using 2-butene-1,4-diol as a starting raw material, and synthesizing the 3-hydroxymethyltetrahydrofuran through a three-step reaction of dehydration cyclization, hydroformylation and reduction. The production technology is moderate in reaction conditions, low in cost, less in three wastes, and suitable for the industrial production.
Robust cobalt oxide catalysts for controllable hydrogenation of carboxylic acids to alcohols
Song, Song,Wang, Dong,Di, Lu,Wang, Chuanming,Dai, Weili,Wu, Guangjun,Guan, Naijia,Li, Landong
, p. 250 - 257 (2018/02/20)
The selective catalytic hydrogenation of carboxylic acids is an important process for alcohol production, while efficient heterogeneous catalyst systems are still being explored. Here, we report the selective hydrogenation of carboxylic acids using earth-abundant cobalt oxides through a reaction-controlled catalysis process. The further reaction of the alcohols is completely hindered by the presence of carboxylic acids in the reaction system. The partial reduction of cobalt oxides by hydrogen at designated temperatures can dramatically enhance the catalytic activity of pristine samples. A wide range of carboxylic acids with a variety of functional groups can be converted to the corresponding alcohols at a yield level applicable to large-scale production. Cobalt monoxide was established as the preferred active phase for the selective hydrogenation of carboxylic acids.
