CAS 70395-35-6

Sodium chlorofluoroacetate

Description:

Sodium chlorofluoroacetate, with the CAS number 70395-35-6, is a chemical compound that belongs to the class of organofluorine compounds. It is characterized by the presence of both chlorine and fluorine atoms attached to an acetate group, which contributes to its unique properties. This compound typically appears as a white crystalline solid and is soluble in water, making it useful in various applications. Sodium chlorofluoroacetate is known for its role as a herbicide and pesticide, functioning by disrupting metabolic processes in target organisms. Its mechanism of action often involves interference with the synthesis of essential biomolecules. Due to its chemical structure, it exhibits stability under normal conditions but may decompose under extreme temperatures or in the presence of strong acids or bases. Safety precautions are necessary when handling this compound, as it can be toxic to non-target organisms, including humans, if ingested or improperly managed. Proper storage and disposal methods are essential to mitigate environmental and health risks associated with its use.

Formula: C₂HClFNaO₂

InChI: InChI=1/C2H2ClFO2.Na/c3-1(4)2(5)6;/h1H,(H,5,6);/q;+1/p-1

SMILES: C(C(=O)O)(Cl)F.[Na]

Sodium chlorofluoroacetate

CAS: 70395-35-6

Formula: C₂HClFNaO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 134.4693

Ref: IN-DA005V6K

Sodium chlorofluoroacetate

CAS: 70395-35-6

Purity: 98%

Molecular weight: 135.47

Ref: 10-F987963

Sodium chloro(fluoro)acetate

CAS: 70395-35-6

Sodium chloro(fluoro)acetate

Formula: C₂HClFO₂·Na

Purity: 98%

Color and Shape: solid

Molecular weight: 134.46931g/mol

Ref: 54-PC3376

Sodium chloro(fluoro)acetate

CAS: 70395-35-6

Sodium chloro(fluoro)acetate (SCCA) is an organofluorine compound that is used in the synthesis of pharmaceuticals, such as silylmethyl and lactam. SCCA has shown to be a selective inhibitor of muscle acetylcholine receptors and is used to study the role of these receptors in muscle contraction. The selectivity of SCCA for brain acetylcholine receptors has also been studied. This agent is effective against tumors and can be used for tumor treatment or therapy. SCCA can be polymerized with dimethylformamide to form polymeric materials that are useful for semiconductor applications. SCCA has been found to have sedative effects and is sometimes used as a hypnotic drug. It also has been found to induce sleep in animals, which may be due to its ability to inhibit the central nervous system’s arousal centers.

Formula: C₂HClFNaO₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 134.47 g/mol

Ref: 3D-FS78889