ChemicalBook--->CAS DataBase List--->1687-29-2

1687-29-2

1687-29-2 Structure

1687-29-2 Structure
IdentificationBack Directory
[Name]

Dimethyl cyclohexane-1,2-dicarboxylate
[CAS]

1687-29-2
[Synonyms]

TIMTEC-BB SBB008381
cis-1,2-Cyclohexanedi
Dimethyl Hexahydrophthalate
DIMETHYL CIS-HEXAHYDROPHTHALATE
imethylcyclohexane-1,2-dicarboxylate
DIMETHYL 1,2-CYCLOHEXANEDICARBOXYLATE
DIMETHYL CYCLOHEXANE-1,2-DICARBOXYLATE
DIMETHYL CIS-1,2-CYCLOHEXANEDICARBOXYLATE
Dimethyl cyclohexane-1,2-dicarboxylate 96%
Dimethylcis-1,2-Cyclohexanedicarboxylate>
(1R,2S)-dimethyl cyclohexane-1,2-dicarboxylate
dimethyl (1S,2R)-cyclohexane-1,2-dicarboxylate
DiMethyl cis-1,2-Cyclohexanedicarboxylate
cis-1,2-Cyclohexanedicarboxylic Acid Dimethyl Ester
cis-Cyclohexane-1,2-dicarboxylic acid dimethyl ester
(1α,2α)-1,2-Cyclohexanedicarboxylic acid dimethyl ester
1,2-Cyclohexanedicarboxylic acid, 1,2-dimethyl ester, (1S,2R)-rel-
[Molecular Formula]

C10H16O4
[MDL Number]

MFCD00043768
[MOL File]

1687-29-2.mol
[Molecular Weight]

200.23
Chemical PropertiesBack Directory
[Boiling point ]

111 °C / 5mmHg
[density ]

1.12
[refractive index ]

1.4570-1.4610
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

clear liquid
[color ]

Colorless to Almost colorless
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P280
[HS Code ]

2917200090
Spectrum DetailBack Directory
[Spectrum Detail]

Dimethyl cyclohexane-1,2-dicarboxylate(1687-29-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Dimethyl phthalate

131-11-3

Dimethyl cyclohexane-1,2-dicarboxylate

1687-29-2

The general procedure for the synthesis of methyl cis-1,2-cyclohexanedicarboxylate from dimethyl phthalate is as follows: the hydrogenation reaction was carried out in a 25 mL stainless steel autoclave with a PTFE liner. In typical operation, 20 mg of catalyst and 61 mg (0.5 mmol) of dimethyl phthalate were dispersed in 5 mL of deionized water. After sealing the autoclave, the air in the autoclave was replaced with hydrogen and pressurized to 2.5 MPa. Under magnetic stirring (1000 rpm), the reaction mixture was heated to 110 °C and maintained until the reaction was completed. At the end of the reaction, it was cooled to room temperature, the reaction mixture was extracted with ethyl acetate and separated by centrifugation to remove the solid catalyst. The recovered solid catalyst was washed sequentially with ethyl acetate, ethanol and deionized water. The filtrate was analyzed by a gas chromatograph (HP5890, USA) equipped with a 30 m HP-5 capillary column and a flame ionization detector (FID). All products were confirmed by gas chromatography-mass spectrometry (Agilent 6890).

[References]

[1] Vysokomolekulyarnye Soedineniya, 1959, vol. 1, p. 349,354
[2] Chem.Abstr., 1960, p. 7217
[3] Applied Catalysis A: General, 2016, vol. 520, p. 73 - 81
[4] RSC Advances, 2017, vol. 7, # 30, p. 18178 - 18188
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