17673-68-6

Basic information

• Product Name: dimethyl (1R,6R)-cyclohex-3-ene-1,6-dicarboxylate
• Synonyms: dimethyl (1R,6R)-cyclohex-3-ene-1,6-dicarboxylate;Dimethyl trans-4-Cyclohexene-1,2-dicarboxylate;trans-4-Cyclohexene-1,2-dicarboxylic Acid Dimethyl Ester;rel-(1R*,2R*)-4-Cyclohexene-1,2-dicarboxylic acid dimethyl ester;Nsc76295;(R,R)-Cyclohex-4-ene-1,2-dicarboxylic acid;Dimethyl trans-4-Cyclohexene-1,2-dicarboxylate;dimethyl trans-cyclohex-4-ene-1,2-dioate
• CAS NO: 17673-68-6
• Molecular Formula: C₁₀H₁₄O₄
• Molecular Weight: 198.22
• Mol File: 17673-68-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 119 °C / 8.5mmHg
• Flash Point: 121.8°C
• Appearance: /
• Density: 1.13
• Vapor Pressure: 0.0137mmHg at 25°C
• Refractive Index: -140 ° (C=1.49, CHCl3)
• CAS DataBase Reference: dimethyl (1R,6R)-cyclohex-3-ene-1,6-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl (1R,6R)-cyclohex-3-ene-1,6-dicarboxylate(17673-68-6)
• EPA Substance Registry System: dimethyl (1R,6R)-cyclohex-3-ene-1,6-dicarboxylate(17673-68-6)

Safety Data

• Hazardous Substances Data: 17673-68-6(Hazardous Substances Data)

Usage

General Description

Dimethyl (1R,6R)-cyclohex-3-ene-1,6-dicarboxylate is a chemical compound that is a derivative of cyclohexene and dicarboxylic acid. It is often used as a reagent in organic synthesis reactions, particularly in the formation of esters and other organic compounds. dimethyl (1R,6R)-cyclohex-3-ene-1,6-dicarboxylate may also have potential applications in pharmaceutical research and development due to its unique structure and reactivity. Additionally, it is important to handle this compound with care, as it may have certain hazards associated with its use, such as flammability and toxicity. Overall, dimethyl (1R,6R)-cyclohex-3-ene-1,6-dicarboxylate is a versatile and potentially useful chemical compound with various industrial and scientific applications.

InChI:InChI=1/C10H14O4/c1-13-9(11)7-5-3-4-6-8(7)10(12)14-2/h3-4,7-8H,5-6H2,1-2H3/t7-,8-/m1/s1

Upstream product

• 25079-83-8 (+/-)-trans-cyclohexene-⁽³⁾-dicarboxylic acid-(1.2) 
• 106-99-0 buta-1,3-diene 
• 624-49-7 dimethylfumarate 
• 4841-84-3 dimethyl cis-1,2,3,6-tetrahydrophthalate 
• 77-79-2 3-Sulfolene 
• 624-48-6 dimethyl cis-but-2-ene-1,4-dioate 
• 1476-11-5 Z-1,4-dichlorobutene 
• 67-56-1 methanol 
• 41183-19-1 trans-4-cyclohexene-1,2-dicarbonyl dichloride 
• 85-43-8 trans-4-Cylohexene-1,2-dicarboxylic anhydride 

Downstream Products

• 173658-51-0 (1R,2R)-cyclohex-4-ene-1,2-dimethanol bis(methansulfonate) 
• 150024-72-9 dimethyl (R,R)-(-)-trans-1,2-cyclohex-4-ene-1,2-dicarboxylate 
• 51025-14-0 (-)-trans-1,2-Dimethyl-cyclohex-4-en 
• 15679-28-4 ((1R,6R)-6-(hydroxymethyl)cyclohex-3-enyl)methanol 
• 14166-21-3 (+/-)-trans-1,2-cyclohexanedicarboxylic anhydride 
• 2305-32-0 trans-1,2-cyclohexanedicarboxylic acid 
• 85-43-8 trans-4-Cylohexene-1,2-dicarboxylic anhydride 
• 96597-06-7 5-Acetoxy-5-(1-acetoxy-ethyl)-2-(1,4-dimethoxy-naphthalen-2-ylmethyl)-cyclohexanecarboxylic acid benzyl ester 
• 95375-34-1 1-(1,4-dimethoxy-3-naphthylmethyl)-2-benzyloxycarbonyl-4-(1-hydroxyethyl)-4-hydroxy-cyclohexane 
• 95375-33-0 1-(1,4-dimethoxy-3-naphthylcarbonyl)-2-methoxycarbonyl-4-acetyl-4-hydroxy-cyclohexane 
• 35079-19-7 trans-(1R,2R)-1,2-Bis(methoxycarbonyl)-4-oxocyclopentane 
• 6453-07-2 (+/-)-trans-4-oxo-1,2-cyclopentanedicarboxylic acid bis(methyl ester) 
• 121369-99-1 5-Acetoxy-5-(1-acetoxy-ethyl)-2-(1,4,8-trimethoxy-naphthalen-2-ylmethyl)-cyclohexanecarboxylic acid 
• 96596-99-5 5-Hydroxy-5-(1-hydroxy-ethyl)-2-(1,4,8-trimethoxy-naphthalen-2-ylmethyl)-cyclohexanecarboxylic acid methyl ester 

Relevant articles and documents

A Change from Kinetic to Thermodynamic Control Enables trans-Selective Stereochemical Editing of Vicinal Diols

Here, we report the selective, catalytic isomerization of cis-1,2-diols to trans-diequatorial-1,2-diols. The method employs triphenylsilanethiol (Ph3SiSH) as a catalyst and proceeds under mild conditions in the presence of a photoredox catalyst and under

Electrochemical Coupling of Activated Olefins and Alkyl Dihalides: Formation of Cyclic Compounds

The electrochemical coupling of dimethyl maleate, methyl cinnamate, 4-phenyl-3-buten-2-one, or methyl acrylate with dibromomethane, 1,3-dibromopropane, 1,4-dibromobutane or other substituted alkyl dihalogenides gave satisfactory yields of cyclic products.The reactions were performed in an undivided cell fitted with a sacrificial aluminum anode, in N-methylpyrrolidone (NMP), at constant current, and at room temperature.The role of the anodically generated metallic ions in this cyclocondensation has been evidenced.