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Sodium-3-(3,5-dimethoxy-4-hydroxyphenyl)-2-propene-1-sulphonate, also known as sodium p-hydroxycinnamate, is a naturally occurring organic compound found in various plants. It is a derivative of cinnamic acid, with a hydroxyl group at the para position and two methoxy groups at the meta positions on the benzene ring. sodium-3-(3,5-dimethoxy-4-hydroxyphenyl)-2-propene-1-sulphonate is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a food additive, particularly as a flavoring agent and preservative, due to its antioxidant properties. The chemical structure of sodium p-hydroxycinnamate consists of a phenyl ring with a hydroxyl group, two methoxy groups, and a sodium sulfonate group attached to a propene chain. Its chemical formula is C11H11O5SNa, and it has a molecular weight of 267.26 g/mol.

7382-63-0

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7382-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7382-63-0 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 7382-63:
(6*7)+(5*3)+(4*8)+(3*2)+(2*6)+(1*3)=110
110 % 10 = 0
So 7382-63-0 is a valid CAS Registry Number.

7382-63-0Downstream Products

7382-63-0Relevant 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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