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Product details
(1R,2R)-(-)-1,2-Cyclohexanedicarboxylic Acid_46022-05-3

(1R,2R)-(-)-1,2-Cyclohexanedicarboxylic Acid

  • CAS:

    46022-05-3

  • English:

    (1R,2R)-(-)-1,2-Cyclohexanedicarboxylic Acid

  • Synonym:

    (1R,2R)-(-)-1,2-Cyclohexanedicarboxylic Acid
    (1R,2R)-1,2-Cyclohexanedicarboxylic Acid
    (1R,2R)-Cyclohexane-1,2-dicarboxylic acid

Details

Chemical Name:(1R,2R)-(-)-1,2-Cyclohexanedicarboxylic Acid
CAS.NO:46022-05-3
Synonyms:(1R,2R)-1,2-Cyclohexanedicarboxylic Acid
(1R,2R)-Cyclohexane-1,2-dicarboxylic acid
Molecular Formula:C8H12O4
Molecular Weight:172.17800
 
Physical and Chemical Properties:
Density:1.315
Melting point:184ºC
Boiling point:384.075ºC
Flash point:200.254ºC
 
Specification:
Appearance:Off-white solid
Assay:≥98.0%
 
Packing:25 kg/drum, can also be packaged according to customer requirements
Storage:Store in a cool, ventilated place
Application:Intermediates of Lurasidone
 
Note:The product under valid patents will not be offered to the countries covered by patents.

By following our guiding principles of Samples, Quotes, Literature, and Innovation, we are able to make continual process improvements for customers.In addition to our core competence in the standard unit operations of organic chemical synthesis, we offer specialised reaction technology, including innovative organometallic synthesis, catalytic transfer hydrogenation and the various operations required for synthesis of chiral compounds.We are a market leader in the development and manufacturing of high performance specialty chemicals. We foster an ambitious culture that focuses on open innovation for new chemical products and business growth.By following our guiding principles of Samples, Quotes, Literature, and Innovation, we are able to make continual process improvements for customers.In addition to our core competence in the standard unit operations of organic chemical synthesis, we offer specialised reaction technology, including innovative organometallic synthesis, catalytic transfer hydrogenation and the various operations required for synthesis of chiral compounds.

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