CAS 29228-15-7

4-Cyclohexene-1,2,3-triol,1-[(benzoyloxy)methyl]-6-chloro-, 3-benzoate, (1S,2S,3R,6S)-

Description:

4-Cyclohexene-1,2,3-triol, 1-[(benzoyloxy)methyl]-6-chloro-, 3-benzoate, with the CAS number 29228-15-7, is a complex organic compound characterized by its cyclohexene ring structure, which features multiple functional groups including hydroxyl (-OH), benzoyloxy, and chloro substituents. This compound is likely to exhibit properties typical of polyhydroxylated compounds, such as increased solubility in polar solvents and potential for hydrogen bonding. The presence of the benzoyloxy group suggests that it may have applications in organic synthesis or as an intermediate in pharmaceutical development. The stereochemistry indicated by the (1S,2S,3R,6S) configuration implies specific spatial arrangements of its substituents, which can influence its reactivity and interactions with biological systems. Additionally, the chloro group may impart unique reactivity patterns, making it a candidate for further chemical transformations. Overall, this compound's structural complexity and functional diversity suggest potential utility in various chemical and medicinal applications.

Formula: C₂₁H₁₉ClO₆

Synonyms:

• Pipoxidechlorohydrin
• 4-Cyclohexene-1,2,3-triol,6-chloro-1-(hydroxymethyl)-, dibenzoate, stereoisomer (8CI)
• 4-Cyclohexene-1,2,3-triol,1-[(benzoyloxy)methyl]-6-chloro-, 3-benzoate, [1S-(1a,2a,3b,6b)]-
• (1S,6α)-1-(Benzoyloxy)methyl-6-chloro-4-cyclohexene-1β,2β,3α-triol 3-benzoate
• 4-Cyclohexene-1,2,3-triol, 1-[(benzoyloxy)methyl]-6-chloro-, 3-benzoate, (1S,2S,3R,6S)-
• Pipoxide chlorohydrin

Pipoxide chlorohydrin

CAS: 29228-15-7

Pipoxide chlorohydrin is a natural product for research related to life sciences. The catalog number is TN6126 and the CAS number is 29228-15-7.

Formula: C₂₁H₁₉ClO₆

Purity: 98%

Color and Shape: Solid

Molecular weight: 402.83

Ref: TM-TN6126

Pipoxide chlorohydrin

CAS: 29228-15-7

Pipoxide chlorohydrin is a synthetic chemical compound, which is derived from the combination of oxides and chlorohydrins through a series of chemical reactions. Its mode of action is primarily characterized by its ability to interact at the molecular level with specific biological pathways, potentially leading to alteration or inhibition of targeted enzymatic processes.

Formula: C₂₁H₁₉ClO₆

Purity: Min. 95%

Molecular weight: 402.8 g/mol

Ref: 3D-EBA22815