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Benzenemethanesulfonic acid, α-ethenyl-4-hydroxy-3-methoxy, monosodium salt, also known as Sodium 3-methoxy-4-hydroxy-alpha-methylstyrene sulfonate, is a chemical compound with the molecular formula C10H11NaO5S. It is a derivative of benzenemethanesulfonic acid, featuring a vinyl group (C2H3), a hydroxyl group (OH), and a methoxy group (OCH3) attached to the benzene ring. Benzenemethanesulfonic acid, a-ethenyl-4-hydroxy-3-methoxy-, monosodium salt is an organic salt, specifically a monosodium salt, which means it contains one sodium ion (Na+) to balance the negative charge of the sulfonic acid group (-SO3H). It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and other organic compounds, due to its unique chemical structure and reactivity.

7382-62-9

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7382-62-9 Usage

Chemical compound

Benzenemethanesulfonic acid, a-ethenyl-4-hydroxy-3-methoxy-, monosodium salt

Physical properties

Crystalline powder, soluble in water

Uses

Precursor in drug synthesis, production of polymers, stabilizer in vinyl polymer emulsions

Properties

Antiseptic and deodorant properties

Applications

Formulation of personal care and cosmetic products

Safety

Can irritate skin, eyes, and respiratory system upon exposure

Check Digit Verification of cas no

The CAS Registry Mumber 7382-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7382-62:
(6*7)+(5*3)+(4*8)+(3*2)+(2*6)+(1*2)=109
109 % 10 = 9
So 7382-62-9 is a valid CAS Registry Number.

7382-62-9Downstream Products

7382-62-9Relevant academic research and scientific papers

Sulphite-promoted delignification of wood: identification of paucidisperse lignosulphonates

Bialski, Alec M.,Luthe, Corinne E.,Fong, Jenny L.,Lewis, Norman G.

, p. 1336 - 1344 (2007/10/02)

Paucidisperse lignosulphonates, previously described as a distinct group of compounds called "hemilignins" (Mw ca. 2000), were conclusively shown to be a complex mixture of monomeric (C9) sulphonic acids.Since these compounds are rapidly solubilized only during the early stages of delignification from softwoods (/= 30percent lignin removal), it can be concluded that they are selectively removed from the secondary wall and not from the middle lamella.This result gives chemical support to the hypothesis that morphological differences in lignin stucture exist.It is proposed that the generation of monolignols and their sulphonated derivatives may occur via an α-O-aryl bond cleavage rather than β-O-aryl cleavage as previously suggested.For softwoods, several other major constituents were isolated, which may be derived from sulphonation of a β-hydroxylated form of coniferyl alcohol.

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