116407-32-0 Usage
Description
(1R,2R)-1,2-Diaminocyclohexane D-tartrate is a chiral compound that serves as a crucial reagent in the synthesis of various materials, particularly in the production of polyimides with a chiral diimine structure. (1R,2R)-1,2-Diaminocyclohexane D-tartrate is characterized by its specific stereochemistry, which is essential for its applications in the chemical and materials science industries.
Uses
Used in Chemical Synthesis Industry:
(1R,2R)-1,2-Diaminocyclohexane D-tartrate is used as a reagent for the synthesis of polyimides containing a chiral diimine. Its unique stereochemistry plays a vital role in the formation of these polymers, which have potential applications in various fields due to their enhanced properties compared to their non-chiral counterparts.
Used in Materials Science:
(1R,2R)-1,2-Diaminocyclohexane D-tartrate is utilized in the development of advanced materials with specific chiral properties. The incorporation of this compound into the synthesis process allows for the creation of materials with improved characteristics, such as enhanced thermal stability, mechanical strength, and optical properties, which can be beneficial in a range of applications, including aerospace, electronics, and biomedical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 116407-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,0 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116407-32:
(8*1)+(7*1)+(6*6)+(5*4)+(4*0)+(3*7)+(2*3)+(1*2)=100
100 % 10 = 0
So 116407-32-0 is a valid CAS Registry Number.
116407-32-0Relevant articles and documents
Preparation method and application of trans-cyclohexanediamine tartrate
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Paragraph 0020-0030, (2019/02/26)
The invention provides a preparation method of trans-cyclohexanediamine tartrate. The preparation method comprises the steps of charging, dropwise adding of trans-cyclohexanediamine, dropwise adding of glacial acetic acid, heat-insulation reaction and cooling. The invention further provides application of the trans-cyclohexanediamine tartrate in preparation of a schiff base metallic cobalt complex. The specific rotation of the prepared trans-cyclohexanediamine tartrate is minus 11 degrees to minus 13 degrees, the content is greater than or equal to 98.0%, and the appearance of the trans-cyclohexanediamine tartrate is off-white or light yellow crystal. The yield of the prepared trans-cyclohexanediamine tartrate is 55.8-56%; and reaction conditions are mild, and the preparation method is simple to operate, is carried out under normal pressure, and is high in safety.