15177-67-0

Basic information

• Product Name: TRANS-1,4-CYCLOHEXANEDICARBOXYLIC ACID MONOMETHYL ESTER
• Synonyms: TRANS-1,4-CYCLOHEXANEDICARBOXYLIC ACID MONOMETHYL ESTER;TRANS-4-CARBOMETHOXYCYCLOHEXANE-1-CARBOXYLIC ACID;4(METHOXY CARBONYL) CYCLOHEXANE CARBOXYLIC ACID;TRANS-4-(METHOXYCARBONYL)CYCLOHEXANECARBOXYLIC ACID;(1r,4r)-4-(methoxycarbonyl)cyclohexanecarboxylic acid;Methyl trans-4-carboxycyclohexane-1-carboxylate;trans-4-(Methoxycarbonyl)cyclohexane-1-carboxylic acid;TRANS-1,4-CYCLOHEXANEDICARBOXYLIC ACID MONOMETHYL
• CAS NO: 15177-67-0
• Molecular Formula: C₉H₁₄O₄
• Molecular Weight: 186.21
• EINECS: 210-614-2
• Product Categories: API
• Mol File: 15177-67-0.mol
• Article Data: 13

Chemical Properties

• Melting Point: 126.0 to 130.0 °C
• Boiling Point: 303.145 °C at 760 mmHg
• Flash Point: 118.334 °C
• Appearance: /
• Density: 1.191 g/cm³
• Vapor Pressure: 0.000219mmHg at 25°C
• Refractive Index: 1.484
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 4.66±0.10(Predicted)
• CAS DataBase Reference: TRANS-1,4-CYCLOHEXANEDICARBOXYLIC ACID MONOMETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: TRANS-1,4-CYCLOHEXANEDICARBOXYLIC ACID MONOMETHYL ESTER(15177-67-0)
• EPA Substance Registry System: TRANS-1,4-CYCLOHEXANEDICARBOXYLIC ACID MONOMETHYL ESTER(15177-67-0)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 15177-67-0(Hazardous Substances Data)

Usage

Uses

Trans-cyclohexane-1,4-dicarboxylic acid monomethyl ester is a carboxylic acid ester derivative, used as organic reagents.

InChI:InChI=1/C9H14O4/c1-13-9(12)7-4-2-6(3-5-7)8(10)11/h6-7H,2-5H2,1H3,(H,10,11)/t6-,7+

Upstream product

• 3399-22-2 dimethyl 1,4-cyclohexanedicarboxylate 
• 94-60-0 dimethyl 1,4-cyclohexane dicarboxylate 
• 619-82-9 trans-hexahydroterephthalic acid 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 120-61-6 1,4-benzenedicarboxylic acid dimethyl ester 
• 186581-53-3 diazomethane 
• 67-56-1 methanol 

Downstream Products

• 183996-92-1 (trans)-4-(2-hydroxypropan-2-yl)cyclohexanecarboxylic acid 
• 4630-82-4 methyl cyclohexylcarboxylate 
• 3399-22-2 dimethyl 1,4-cyclohexanedicarboxylate 
• 127946-00-3 1,3-dipropyl-8-(trans-4-carboxycyclohexyl)xanthine 
• 32529-80-9 4-methoxycarbonylcyclohexanecarbonyl chloride 
• 110928-44-4 trans-(4-hydroxymethyl)cyclohexane-1-carboxylic acid methyl ester 
• 1224871-31-1 4-{4-[5-(3-tert-butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carbonyl}-cyclohexanecarboxylic acid methyl ester 
• 936901-99-4 Methyl trans-4-{[(2,5-dioxopyrrolidin-1-yl)oxy]carbonyl}cyclohexanecarboxylate 
• 1005502-63-5 trans-4-(2-fluoro-benzoyl)-cyclohexanecarboxylic acid methyl ester 
• 1345045-52-4 trans-4-(3-fluoro-pyridine-4-carbonyl)-cyclohexanecarboxylic acid methyl ester 
• 1345045-51-3 trans-4-(3-fluoro-pyridine-2-carbonyl)-cyclohexanecarboxylic acid methyl ester 
• 1345045-53-5 trans-4-(2-chloro-pyridine-3-carbonyl)-cyclohexanecarboxylic acid methyl ester 
• 1345045-64-8 trans-4-(2-benzylsulfanyl-benzoyl)-cyclohexanecarboxylic acid methyl ester 
• 1345045-67-1 trans-4-benzo[d]isothiazol-3-yl-cyclohexanecarboxylic acid methyl ester 

Relevant articles and documents

Magnetic Field Dependent Reaction Yields from Radical Ion Pairs Linked by a Partially Rigid Aliphatic Chain

The electron donor-acceptor compound pyrene-(CH2)3-cyclohexane-(CH2)3-dimethylaniline, abbreviated as Py3(C6)3DMA, has been investigated.Photoinduced electron transfer leads to the singlet radical ion pair Py-3(C6)3DMA+.An extraordinary large and distinct magnetic field effect is observed in the yield of the locally excited triplet state of the pyrene moiety, the recombination product of the triplet radical ion pair.The half-width of the "J-resonance" maximum in the magnetic field dependent triplet yield curve is just 66 G, corresponding to 7.7*10-7 eV or 6.2*10-3 cm-1.This is due to the influence of the rigid trans-cyclohexane part in the aliphatic chain, which leads to a reduced intramolecular mobility and to a narrow probability distribution of the radical ion pair distance, as predicted by Monte-Carlo computer simulations.The magnetic field dependence of the triplet generation is further transmitted to secondary reactions like triplet-triplet annihilation, thus leading to a magnetic field dependent delayed fluorescence and to a delayed excimer fluorescence.

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Provided herein are compounds and methods for modulating abnormal repeat expansions of gene sequences. More particularly, provided are inhibitors of RNA and the uses of such inhibitors in regulating nucleotide repeat expansions, e.g., to treat Myotonic Dystrophy Type 1 (DM1 ), Myotonic Dystrophy Type 2 (DM2), Fuchs dystrophy, Huntington Disease, Amyotrophic Lateral Sclerosis, or Frontotemporal Dementia.

Polymerizable compound, composition, polymer, an optically anisotropic material, an organic EL element and a liquid crystal display element

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