CAS 23635-14-5
:(4S)-4-(1-methylethenyl)cyclohex-1-ene-1-carboxylate
Description:
The chemical substance known as (4S)-4-(1-methylethenyl)cyclohex-1-ene-1-carboxylate, with the CAS number 23635-14-5, is an organic compound characterized by its cyclohexene structure, which features a carboxylate functional group and a vinyl substituent. This compound is typically a colorless to pale yellow liquid with a distinctive odor, indicative of its unsaturated nature. Its molecular structure includes a cyclohexene ring, which contributes to its reactivity and potential applications in organic synthesis. The presence of the carboxylate group suggests that it may participate in various chemical reactions, such as esterification or nucleophilic substitutions. Additionally, the stereochemistry indicated by the (4S) configuration implies specific spatial arrangements that can influence its biological activity and interactions. This compound may be of interest in fields such as fragrance chemistry, agrochemicals, or as an intermediate in the synthesis of more complex molecules. As with many organic compounds, safety data sheets should be consulted for handling and storage guidelines.
Formula:C10H13O2
InChI:InChI=1/C10H14O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h5,8H,1,3-4,6H2,2H3,(H,11,12)/p-1/t8-/m1/s1
SMILES:C=C(C)[C@@H]1CC=C(CC1)C(=O)[O-]
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Found 4 products.
(S)-4-(Prop-1-En-2-Yl)Cyclohex-1-Enecarboxylic Acid
CAS:(S)-4-(Prop-1-En-2-Yl)Cyclohex-1-Enecarboxylic AcidPurity:99%Molecular weight:166.22g/mol(S)-(-)-Perillic acid
CAS:S)-(-)-Perillic acid is a terpenoid natural product capable of inhibiting protein pentosylisation and protein acylation, anti-infective and anti-cancer.Formula:C10H14O2Color and Shape:SolidMolecular weight:166.22Perillic Acid
CAS:Perillic Acid is a cytotoxic compound that has been shown to have minimal toxicity. It is a natural product found in the perilla plant and has been shown to be effective at inhibiting the growth of skin cancer cells. Perillic acid blocks the activity of the α1 subunit, which inhibits the production of growth factor-β1 and c-jun phosphorylation. The compound also induces apoptosis in cancer cells by binding to the wild-type strain and inhibiting DNA synthesis. The anticancer effects of perillic acid have been demonstrated in cell cultures from carcinoma cell lines.Formula:C10H14O2Purity:Min. 95%Molecular weight:166.22 g/mol



