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1622-67-9

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1622-67-9 Usage

General Description

"1,5-dihydro-3-isopropyl-8-methyl-[1,3]dioxepino[5,6-c]pyridin-9-ol" is a chemical compound with a complex molecular structure. It consists of a 1,3-dioxepane ring fused to a pyridine ring, with a hydroxyl group attached at the 9th position. The presence of an isopropyl and a methyl group in the molecule adds to its complexity. This chemical may have potential applications in pharmaceutical or industrial settings, but further research would be needed to determine its specific properties and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 1622-67-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1622-67:
(6*1)+(5*6)+(4*2)+(3*2)+(2*6)+(1*7)=69
69 % 10 = 9
So 1622-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO3/c1-7(2)12-15-5-9-4-13-8(3)11(14)10(9)6-16-12/h4,7,12,14H,5-6H2,1-3H3

1622-67-9Relevant articles and documents

New synthetic route of vitamine B6

Miki,Matsuo

, p. 323 - 325 (1967)

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MANUFACTURE OF VITAMIN B6

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Page/Page column 14, (2008/06/13)

A process for manufacturing a 3-unsubstituted, 3-monosubstituted or 3,3-disubstituted 9-acyloxy-1,5-dihydro-8--methylpyrido[3,4-e] [1,3]dioxepin (I) and optionally for manufacturing pyridoxine involves performing an addition reaction between a 4-methyl-5-alkoxy-oxazole (II) and a 2-unsubstituted, 2-monosubstituted or 2,2-disubstituted 4,7-dihydro-(1,3)-dioxepin (III) in the substantial absence of a solvent and a catalyst to give a product mixture consisting essentially of the appropriate Diels-Alder adduct (IV) in a major proportion and the appropriate 3--unsubstituted, 3-monosubstituted or 3,3-disubstituted 1,5-dihydro-8-methylpyrido[3,4-e] [1,3]dioxepin 9-ol (V) in a minor proportion, removal of a substantial proportion of the unreacted oxazole and dioxapin starting materials from the product mixture by distillation under reduced pressure, addition of a substantially anhydrous organic acid to said product mixture and rearrangement of the Diels-Alder adduct IV to further V in the presence of said substantially anhydrous organic acid with removal of the generated alkanol by distillation under reduced pressure, and acylation of the resultingly enriched quantity of V with an added carboxylic acid anhydride to produce the desired I, and optionally converting this so-manufactured acylation product I to pyridoxine by acid hydrolysis for achieving deprotection and deacylatiom. Pyridoxine is a well known form of vitamin B6 with well established utility.

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