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140459-96-7

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140459-96-7 Usage

Description

(1R.2R)-DIMETHYL CYCLOHEXANE-1,2-DICARBOXYLATE, also known as (1R,2R)1,2-Cyclohexanedicarboxylic Acid 1,2-Dimethyl Ester, is an organic compound with a unique cyclohexane structure featuring two ester groups and a dimethyl substitution. It is characterized by its chemical stability and reactivity, making it a valuable intermediate in various chemical syntheses.

Uses

Used in Chemical Synthesis:
(1R.2R)-DIMETHYL CYCLOHEXANE-1,2-DICARBOXYLATE is used as a chemical reagent for the synthesis of advanced tetracyclic systems. Its unique structure and reactivity allow for the creation of complex molecular architectures that are essential in the development of new pharmaceuticals, materials, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1R.2R)-DIMETHYL CYCLOHEXANE-1,2-DICARBOXYLATE is used as a key intermediate in the synthesis of various drug candidates. Its ability to form complex tetracyclic systems makes it a valuable component in the development of novel therapeutic agents with improved efficacy and selectivity.
Used in Material Science:
(1R.2R)-DIMETHYL CYCLOHEXANE-1,2-DICARBOXYLATE is also utilized in the field of material science for the development of advanced polymers and other materials with unique properties. Its incorporation into these materials can lead to enhanced performance characteristics, such as increased strength, durability, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 140459-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,4,5 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 140459-96:
(8*1)+(7*4)+(6*0)+(5*4)+(4*5)+(3*9)+(2*9)+(1*6)=127
127 % 10 = 7
So 140459-96-7 is a valid CAS Registry Number.

140459-96-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl (1R,2R)-1,2-cyclohexanedicarboxylate

1.2 Other means of identification

Product number -
Other names trans-Cyclohexan-dicarbonsaeure-1,2-dimethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:140459-96-7 SDS

140459-96-7Relevant articles and documents

The Construction of Homochiral Lanthanide Quadruple-Stranded Helicates with Multiresponsive Sensing Properties toward Fluoride Anions

Chen, Wanmin,Tang, Xiaoliang,Dou, Wei,Wang, Bei,Guo, Lirong,Ju, Zhenghua,Liu, Weisheng

, p. 9804 - 9811 (2017)

A series of unique homochiral lanthanide tetranuclear quadruple-stranded helicates have been self-assembled controllably by using the intrinsic advantages of chiral bridging ligands, (S)-H2L and (R)-H2L, and lanthanide ions with high coordination numbers. The self-assembly process of these chiral helicates not only ensures the structural stability and quadruple-stranded feature of lanthanide cluster in the solid state and solution, but also achieves effective transfer and amplification of the chirality code from the ligand to a higher supramolecular level. Moreover, through using optical rotation, circular dichroism spectra analysis, and luminescence measurements, we demonstrate that these chiral lanthanide helicates could serve as sensitive and multi-responsive sensors to recognize and detect F? anions based on the change of chiral signal and NIR luminescence simultaneously, which represents a meaningful exploration for developing functional lanthanide-based polynuclear clusters.

Synthesis of phthalate-free plasticizers by hydrogenation in water using RhNi bimetallic catalyst on aluminated SBA-15

Phan-Vu, Duc-Ha,Tan, Chung-Sung

, p. 18178 - 18188 (2017/04/04)

In this study, rhodium-nickel bimetallic nanoparticles loaded on aluminated silica (RhNi/Al-SBA-15) were used as catalysts for the hydrogenation of phthalate in water to produce environmentally acceptable non-phthalate plasticizers. Chemical fluid deposition (CFD) was used to dope metals onto the aluminated silica support, which helped to create a uniform structure of RhNi on Al-SBA-15. The introduction of Ni helped to reduce the use of expensive Rh and increase the number of metal active sites by reducing the bimetallic nanoparticle size. Aluminated SBA-15 not only acted as the support for the RhNi bimetallic catalyst but also enhanced the reaction efficiency by introducing Br?nsted and Lewis acid sites and the absorption of phthalates on the catalyst in water. The physicochemical properties of prepared catalysts were characterized by N2 adsorption-desorption isotherm, X-ray diffraction (XRD), in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), Scanning electron microscopy (SEM), and Transmission electron microscopy (TEM). The catalytic performance of the synthesized catalysts was evaluated with the hydrogenation of dimethyl phthalate (DMP). Despite the low solubility of DMP in water, the hydrogenation using Rh0.5Ni1.5/Al-SBA-15 was carried out with an 84.4% reaction yield (cis-?:?trans- = 97.5?:?2.5) at 80 °C using 1000 psi of H2 after 2 h.

Based on the chiral diamine spiro skeleton chiral phosphorus nitrile catalyst, preparation method and application thereof

-

Paragraph 0153; 0154, (2017/08/16)

The invention provides a chiral phosphazene catalyst based on a spiro framework adopting chiral diamine, a preparation method and an application of the chiral phosphazene catalyst. The catalyst has a structure represented in the general formula: (RX-)3P=NR', chiral groups are introduced through R and R', and the catalyst has a structure with two seven-membered rings in centered connection through phosphorspirol. Optically pure tartaric acid or substituted hexahydrophthalic acid or 1,2-cyclopentanedicarboxylicacid,(1R,2S)-rel- is taken as a raw material, chiral diamine is generated through esterification, a Grignard reaction, an optional chlorination reaction, an azido reaction and a reduction reaction of the raw material, then chiral diamine and phosphorus pentachloride have a spirocyclization reaction to construct a phosphorspirol-centered screw ring, the chiral phosphazene molecular catalyst is obtained under the alkaline condition, and a method for substituting azido for hydroxyl directly has good application and popularization value. The catalyst has the advantages of high catalysis efficiency, good stereoselectivity, mild conditions, economy, environmental protection, simplicity and convenience in operation and the like as well as popularization and application prospects.

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