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(1S,3R)-(−)-Camphoric acid / 1 G

Purity: 99 %
Synonym: (−)-Camphoric acid; (1S,3R)-1,2,2-Trimethyl-1,3-cyclopentanedicarboxylic acid; L-Camphoric Acid
Molecular Formula: C10H16O4
Molecular Weight: 200.23
SKU: MND-53744
CAS Number: 560-09-8
MDL number: MFCD00064937
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Packing size: 1 G  
160.30 EUR


Properties

Flash Point (C)Not available
Flash Point (F)Not available
Melting Point188-190 °C (lit.)

 Product Description

(1S,3R)-(−)-Camphoric acid is a chiral compound with a specific stereochemical arrangement. It is commonly employed in organic synthesis, serving as a key intermediate for the production of pharmaceuticals, agrochemicals, and fine chemicals.

 

Application:

Utilized in organic chemistry, (1S,3R)-(−)-Camphoric acid acts as a crucial building block for the synthesis of various chemical compounds. Its application is particularly significant in the manufacturing of pharmaceuticals, agrochemicals, and fine chemical products.

 

 

Articles:

- 1 D Supramolecular Double-Chains based on π-π Stacking Interactions: Synthesis and Crystal Structure of [Cu(phen)(C10H16O4)] · 3 H2O with phen = 1,10-phenanthroline

Publication Date: 16 May 2000

Yue-Qing Zheng Prof. Dr., Jie Sun, Jian-Li Lin

https://doi.org/10.1002/(SICI)1521-3749(200006)626:6<1274::AID-ZAAC1274>3.0.CO;2-J

 

- Crystal structure and phase transition of bis-aqua-sebacato magnesium Mg(C10H16O4)2(H2O)2

Publication Date: Available online 18 May 2011

Adel Mesbah, Lionel Aranda, Jean Steinmetz, Emmanuel Rocca, Michel François

https://doi.org/10.1016/j.solidstatesciences.2011.05.008

 

- (1R,3S)-Camphoric acid as a building block in supramolecular chemistry: adducts with organic polyamines

Publication Date: 2003

C. M. Zakaria, G. Ferguson, A. J. Lough and C. Glidewell

https://doi.org/10.1107/S0108768102022358