25357-95-3

Basic information

• Product Name: 1,3,5-CYCLOHEXANETRICARBOXYLIC ACID
• Synonyms: 1,3,5-CYCLOHEXANETRICARBOXYLIC ACID;CYCLOHEXANE-1,3,5-TRICARBOXYLIC ACID;1,3,5-Cyclohexanetricarboxylic Acid (cis- and trans- mixture);1,3,5-Cyclohexanetricarboxylic Acid (cis- and trans- mixture);1,3,5-Cyclohexanetricarboxylic acid cis 95 %
• CAS NO: 25357-95-3
• Molecular Formula: C₉H₁₂O₆
• Molecular Weight: 216.19
• Product Categories: pharmacetical;Building Blocks for Dendrimers;Functional Materials
• Mol File: 25357-95-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 207 °C
• Boiling Point: 372.4°Cat760mmHg
• Flash Point: 193.2°C
• Appearance: /
• Density: 1.509g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.555
• PKA: 3.72±0.26(Predicted)
• CAS DataBase Reference: 1,3,5-CYCLOHEXANETRICARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-CYCLOHEXANETRICARBOXYLIC ACID(25357-95-3)
• EPA Substance Registry System: 1,3,5-CYCLOHEXANETRICARBOXYLIC ACID(25357-95-3)

Safety Data

• Hazardous Substances Data: 25357-95-3(Hazardous Substances Data)

Usage

General Description

1,3,5-Cyclohexanetricarboxylic acid is a chemical compound with the molecular formula C9H14O6. It is a tricarboxylic acid derivative of cyclohexane and features three carboxylic acid functional groups. It is a white, crystalline solid that is sparingly soluble in water and has a melting point of 220-222 degrees Celsius. It is primarily used as a precursor for the synthesis of various pharmaceuticals and agrochemicals. Additionally, it is used in the production of specialty polymers and as a chelating agent in coordination chemistry. It is also known to have potential applications in the field of medicine, particularly in the treatment of certain diseases and disorders.

InChI:InChI=1/C9H12O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h4-6H,1-3H2,(H,10,11)(H,12,13)(H,14,15)/t4-,5+,6-

Upstream product

• 554-95-0 benzene-1,3,5-tricarboxylic acid 

Downstream Products

• 74421-59-3 1,3,5-cyclohexanetrimethylamine 

Relevant articles and documents

Alicyclic carboxylic acid

PROBLEM TO BE SOLVED: To provide an unprecedentedly efficient method for manufacturing an alicyclic carboxylic acid by using a ruthenium-palladium co-supported catalyst as a catalyst for hydrogenating aromatic rings of aromatic carboxylic acids.SOLUTION:

Optically active phenoxypropionic esters

Optically active compounds of the formula I STR1 where R is C1 -C12 -alkyl or -perfluoroalkyl in which one or two non-adjacent CH2 or CF2 groups can also be replaced by --O-- and/or --CO-- and/or --CO--O-- and/or --CH=CH-- and/or --CH-halogen-- and/or --CHCN-- and/or --0--CO--CH-halogen-- and/or --O--CO--CHCN--, or is C1 -C12 -alkyl which can have a terminal chemically reactive group and in which a CH2 group can be replaced by --O--, A1 and A2 are each, independently of one another, 1,4-phenylene which is unsubstituted or substituted by one or two F and/or Cl and/or Br atoms and/or CH3 groups and/or CN groups and in which one or two CH groups can also be replaced by N, 1,4-cyclohexylene in which one or two non-adjacent CH2 groups can also be replaced by --O-- and/or --S--, 1,4-piperidinediyl, 1,4-bicyclo[2.2.2]octylene, 2,6-naphthalenediyl, decahydro-2,6-naphthalenediyl or 1,2,3,4-tetrahydro-2,6-naphthalenediyl, A3 is unsubstituted or substituted phenyl, Z is --CO--O--, --O--CO--, --CH2 CH2 --, --OCH2 --, --CH2 O--, --C C-- or a single bond and m is 0, 1, 2 or 3.