2658-60-8

Usage

Uses

Used in Polymer Production:
Cyclohexane-1,1-dimethanol is used as a monomer in the production of various polymers, such as polyesters and polyurethanes, for its ability to enhance the chemical and solvent resistance, as well as the low volatility of the resulting materials.
Used in Automotive Industry:
In the automotive industry, Cyclohexane-1,1-dimethanol is used as a component in the manufacturing of high-performance materials for various applications, such as engine components and protective coatings, due to its excellent resistance to chemicals and solvents.
Used in Construction Industry:
Cyclohexane-1,1-dimethanol is utilized in the construction industry as a key ingredient in the production of durable materials for building and infrastructure projects, taking advantage of its resistance to chemicals and solvents, as well as its low volatility.
Used in Textile Industry:
In the textile industry, Cyclohexane-1,1-dimethanol is employed in the manufacturing of high-performance and durable fabrics, leveraging its unique properties to create materials with enhanced resistance to chemicals and solvents, making them suitable for various applications, such as protective clothing and industrial textiles.

InChI:InChI=1/C8H16O2/c9-6-8(7-10)4-2-1-3-5-8/h9-10H,1-7H2

Upstream product

• 1139-13-5 diethyl cyclohexane-1,1-dicarboxylate 
• 2160-94-3 4,4-bis(hydroxylmethyl)cyclohexene 
• 50-00-0 formaldehyd 
• 2043-61-0 cyclohexanecarbaldehyde 
• 15719-64-9 methylammonium carbonate 
• 124-38-9 carbon dioxide 
• 111-24-0 1,5-dibromo-pentane 
• 4630-82-4 methyl cyclohexylcarboxylate 
• 79-22-1 methyl chloroformate 
• 24632-01-7 1-hydroxymethylcyclohexane carbaldehyde 

Downstream Products

• 99169-13-8 1,1-bis-chlorocarbonyloxymethyl-cyclohexane 
• 94073-94-6 1,1-bis-carbamoyloxymethyl-cyclohexane 
• 21623-88-1 1,1-bis-bromomethyl-cyclohexane 
• 1127-08-8 cyclohexanedicarboxylic acid 
• 62161-66-4 1,1-bis-methanesulfonyloxymethyl-cyclohexane 
• 2658-61-9 1,1-bis-benzenesulfonyloxymethyl-cyclohexane 
• 22308-11-8 cyclohexane-1,1-diylbis(methylene)bis(4-methylbenzenesulfonate) 
• 169207-04-9 1,1-Bis<<(trifluoromethanesulfonyl)oxy>methyl>cyclohexane 
• 185-13-7 2-selena-spiro[3.5]nonane 
• 1345335-76-3 1,1-bis[(ethenyloxy)methyl]cyclohexane 
• 1276693-09-4 C₁₁H₂₀O₂ 
• 185-11-5 2-thiaspiro[3.5]nonane 
• 56472-19-6 1,1-bis(mercartomethyl)cyclohexane 

Relevant academic research and scientific papers

GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with a defect in glyoxylate metabolism, for example a disease or disorder associated with the enzyme glycolate oxidase (GO) or alterations in oxalate metabolism. Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.

GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with the enzyme glycolate oxidase (GO). Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.

METHOD FOR PRODUCING DIOL

PROBLEM TO BE SOLVED: To provide a method for producing a diol having two methylol groups at one carbon atom on an alicyclic skeleton, which is inexpensive and generates a small amount of waste. SOLUTION: There is provided a method for producing a diol re

TRICYCLIC COMPOUND SERVING AS IMMUNOMODULATOR

Provided are compounds of formula I and formula II or pharmaceutically acceptable salts of the compounds and pharmaceutical compositions thereof. The compounds of formula I and formula II or the pharmaceutically acceptable salts of the compounds provide indole 2,3-dioxygenase (IDO) inhibitory activity and are capable of treating IDO-mediated immunosuppressive diseases, such as infectious diseases or cancer.

Diverse ring opening of thietanes and other cyclic sulfides: An electrophilic aryne activation approach

Organosulfides are a common class of structure units in bioactive molecules and functional materials motivating continuous developments of efficient synthetic methods. Herein, we report an electrophilic aryne-activated ring opening protocol of one or two

METHOD FOR PRODUCING DIOL

PROBLEM TO BE SOLVED: To provide a method for producing a diol having an aliphatic ring skeleton in high yield, while avoiding viscosity increase of a reaction system, sudden heat generation and thermal runaway chemical reaction. SOLUTION: There is provid

1,1-BIS[(ETHENYLOXY)METHYL]CYCLOHEXANE AND METHOD OF PRODUCTION OF SAME

A novel compound, 1,1-bis[(ethenyloxy)methyl]cyclohexane having the formula (I) and having a low odor, low volatility and low skin irritability, which is useful as a starting material for a polymerization composition having a low toxicity and excellent cu

BENZISOXAZOLE COMPOUND

Disclosed is a compound represented by the general formula (I) or a salt thereof: wherein any one of R1, R2 and R3 represents a group represented by the formula: -(CH2)m-NR11R12 (wherein m is 1 or 2; and R11 and R12 independently represent a hydrogen atom or a C1-6 alkyl group or may, together with a nitrogen atom to which R11 and R12 are bound, form a 4- or 5-membered cyclic group); the remaining two or R1, R2 and R3 independently represent a group represented by the formula: -(O)n-R21 (wherein n is 0 or 1; and R21 represents a hydrogen atom, a C1-6 alkyl group, a C2-6 alkenyl group, a C2-6 alkynyl group, or the like); and R4 represents a C1-6 alkyl group which may have a substituent or the like.

Preparation of di- and polynitrates by ring-opening nitration of oxetanes by dinitrogen pentoxide (N2O5)

Ten oxetanes bearing various substituents were reacted with N2O5 in chlorinated hydrocarbon solvents to yield 1,3-dinitrate esters (I) by ring-opening nitration. The yields ranged from 73 to 88% for di-/trinitrates derived from oxetanes unsubstituted in the 2-position, to only 15 to 21% for oxetanes bearing such substituents. Although selective ring cleavage of oxetanes bearing non-hydroxylic substituents (epoxy (oxiranyl), spiro-oxetane and alkene) was not, in general, possible, selective nitration of hydroxyalkyloxetanes was achievable under the conditions employed to yield nitrato-methyloxetanes useful as precursors for energetic polyethers. A semi-quantitative reactivity comparison with representative epoxides indicated that the reactivity of oxetanes towards N2O5 was lower, as expected on account of their lower ring strain.

Laser-Powered Decomposition of Spiroalkanes (n = 2-5)

The laser heating of spiroalkanes (n=2-5) and of their 1,1,2,2-tetradeuterated isotopomers reveals dissimilar modes of their thermal decomposition.Spiropentane decomposes into ethene and propadiene via two competing routes: the direct cleavage and the more important cleavage via intermediary methylenecyclobutane.Spirohexane decomposes through two important concurrent pathways which are the expulsions of ethene from the three-membered ring and a more feasible expulsion of ethene from the four-membered ring.Spiroheptane and spirooctane decompose by a radical-chain mechanism and afford complex mixtures of products; upon addition of propene both compounds rearrange into two cycloalkanes wherein the larger ring of the spiroalkane is preserved and substituted with ethylidene and a vinyl group.