2305-31-9

Basic information

• Product Name: cis-1,3-cyclohexanedicarboxylic acid
• Synonyms: 1,3-Cyclohexanedicarboxylicacid, (1R,3S)-rel-;cis-Cyclohexane-1,3-dicarboxylic acid;cis-1,3-Cyclohexanedicarboxylic Acid;(1S*,3R*)-Cyclohexane-1,3-dicarboxylic acid
• CAS NO: 2305-31-9
• Molecular Formula: C₈H₁₂O₄
• Molecular Weight: 172.18
• Mol File: 2305-31-9.mol
• Article Data: 9

Chemical Properties

• Melting Point: 165 °C
• Boiling Point: 332.4°Cat760mmHg
• Flash Point: 169°C
• Appearance: /
• Density: 1.314g/cm³
• Vapor Pressure: 2.83E-05mmHg at 25°C
• Refractive Index: 1.521
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: cis-1,3-cyclohexanedicarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: cis-1,3-cyclohexanedicarboxylic acid(2305-31-9)
• EPA Substance Registry System: cis-1,3-cyclohexanedicarboxylic acid(2305-31-9)

Safety Data

• Hazardous Substances Data: 2305-31-9(Hazardous Substances Data)

Usage

General Description

Cis-1,3-Cyclohexanedicarboxylic acid is an organic compound that belongs to the class of cyclic dicarboxylic acids. This chemical is characterized by its two carboxylic acid functional groups (-COOH) and a cyclohexane ring structure. The "cis" in its name refers to the spatial arrangement of the carboxylic acid groups that are on the same side of the cyclohexane ring. It is often used in the synthesis of other organic compounds, polymers, and in biochemical research. The acid has a relatively high melting point, and it's slightly soluble in water. With a variety of industrial and scientific applications, cis-1,3-cyclohexanedicarboxylic acid plays a crucial role in chemical manufacture and research.

InChI:InChI=1/C8H12O4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h5-6H,1-4H2,(H,9,10)(H,11,12)/t5-,6+

Upstream product

• 22605-65-8 cis-1,3-cyclohexanedicarbonyl chloride 
• 98558-90-8 6,6-Dihydroxy-bicyclo-<1.1.3>-heptan-carbonsaeure-(1) 
• 101499-78-9 Bicyclo-<1.1.3>-heptanon-(6)-yl-(1)-ester der 6.6-Dihydroxy-bicyclo-<1.1.3>-heptan-carbonsaeure-(1) 
• 121-91-5 isophthalic acid 
• 4355-31-1 3-oxabicyclo<3.3.1>nonane-2,4-dione 
• 1610728-91-0 (S,S)-dibenzyl cyclohexyl 1,3-dicarboxylate 
• 110333-10-3 C₁₀H₁₂O₄ 
• 98490-87-0 Bicyclo-<1.1.3>-heptanon-(6)-carbonsaeure-(1)-chlorid 
• 100378-67-4 Bicyclo-<1.1.3>-heptanon-(6)-carbonsaeure-(1) 
• 1165952-92-0 cyclohexa-1,4-diene 
• 109559-41-3 1,1,3,3-tetraethoxycarbonylcyclohexane 
• 626-15-3 1,3-bis-(bromomethyl)benzene 
• 77976-01-3 2,4-dimethoxybicyclo<3.3.1>nona-9-one 
• 79692-86-7 2,4-dimethoxybicyclo<3.3.1>nonane 

Downstream Products

• 6998-82-9 dimethyl cis-1,3-cyclohexanedicarboxylate 
• 3725-17-5 1,3-dibromocyclohexane 
• 1610729-37-7 N-(5-((1S,3S)-3-(5-amino-1,3,4-thiadiazol-2-yl)cyclohexyl)-1,3,4-thiadiazol-2-yl)-2-(pyridin-2-yl)acetamide 
• 1610727-94-0 N-(5-((1S,3S)-3-(5-acetamido-1,3,4-thiadiazol-2-yl)cyclohexyl)-1,3,4-thiadiazol-2-yl)-2-(3-methoxyphenyl)acetamide 
• 1610728-92-1 5,5'-((1S,3S)-cyclohexane-1,3-diyl)bis(1,3,4-thiadiazol-2-amine) 
• 280-70-6 3-azabicyclo<3.3.1>nonane 
• 161117-17-5 (1S,3R)-Cyclohexane-1,3-dicarbonyl difluoride 
• 116724-13-1 trans rac-cyclohexyl 1,3-dicarboxylic acid 
• 26772-34-9 (1R,3S)-cyclohexane-1,3-diamine 
• 40098-81-5 cis-1,3-cyclohexanediacetic acid 
• 22605-65-8 cis-1,3-cyclohexanedicarbonyl chloride 
• 62059-56-7 cis-1,3-Cyclohexanedicarboxylic acid diethyl ester 

Relevant articles and documents

Search for a predicted hydrogen bonding motif - A multidisciplinary investigation into the polymorphism of 3-azabicyclo[3.3.1]nonane-2,4-dione

The predictions of the crystal structure of 3-azabicyclo[3.3.1]nonane-2,4- dione submitted in the 2001 international blind test of crystal structure prediction (CSP2001) led to the conclusion that crystal structures containing an alternative hydrogen bond

Highly-efficient Ru/Al-SBA-15 catalysts with strong Lewis acid sites for the water-assisted hydrogenation of: P -phthalic acid

Ruthenium nanoparticles supported onto aluminum-doped mesoporous silica catalysts (Ru/Al-SBA-15) are fabricated using hydrothermal and impregnation methods for catalysis application. The Ru/Al-SBA-15-3 catalyst at a Si/Al molar ratio of 3 exhibited excellent catalytic performance for the hydrogenation of p-phthalic acid with high conversion efficiency (100.0%) and cis-isomer selectivity (84.0%) in water. Moreover, this system displays exceptional stability and recyclability through preserving the conversion efficiency, as well as a cis-isomer selectivity of 90.2 and 83.3%, respectively, after reusing it fourteen times. Such an exceptional system can also be ideal for the hydrogenation of aromatic dicarboxylic acids and their ester derivatives in water. Strong Lewis acid sites due to doped Al species play significant roles in the hydrogenation reaction. Moreover, isotope labeling studies indicated that water molecules effectively participated in the hydrogenation reaction. Hydrogen and water contributed half of the hydrogen atoms for this hydrogenation reaction. In the end, a plausible mechanistic pathway for the hydrogenation of p-phthalic acid using the Ru/Al-SBA-15-3 catalyst in water is proposed.

COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES AS GLUTAMINASE INHIBITORS FOR TREATING CANCERS THEREOF

Provided are compounds of formula (I), wherein X, Y, Z, W, m, n, o, p, R1, R2 and R6 are defined as in the description. Pharmaceutical compositions and uses as glutaminase inhibitors for treating cancers thereof are also provided.

Efficient and Practical Arene Hydrogenation by Heterogeneous Catalysts under Mild Conditions

An efficient and practical arene hydrogenation procedure based on the use of heterogeneous platinum group catalysts has been developed. Rh/C is the most effective catalyst for the hydrogenation of the aromatic ring, which can be conducted in iPrOH under neutral conditions and at ordinary to medium H 2 pressures (10 atm). A variety of arenes such as alkylbenzenes, benzoic acids, pyridines, furans, are hydrogenated to the corresponding cyclohexyl and heterocyclic compounds in good to excellet yields. The use of Ru/C, less expensive than Rh/C, affords an effective and practical method for the hydrogenation of arenes including phenols. Both catalysts can be reused several times after simple filtration without any significant loss of catalytic activity.