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Acetic acid-[3,7-dimethyl-9-((Ξ)-2,6,6-trimethyl-cyclohex-2-enylidene)-nona-3ξ,5t,7ξ-trienyl ester] is a complex organic compound with a long and intricate chemical structure. It is an ester derivative of acetic acid, where the hydroxyl group of acetic acid is replaced by a long alkenyl chain containing three double bonds and various methyl groups. The compound's structure is characterized by a cyclohexene ring and a nonatriene chain, which contribute to its unique chemical properties and potential applications in various fields, such as pharmaceuticals, fragrances, or chemical research. Due to its complexity, acetic acid-[3,7-dimethyl-9-((Ξ)-2,6,6-trimethyl-cyclohex-2-enylidene)-nona-3ξ,5t,7ξ-trienyl ester] is typically synthesized through multi-step reactions and requires careful handling and analysis.

7631-44-9

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7631-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7631-44-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,3 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7631-44:
(6*7)+(5*6)+(4*3)+(3*1)+(2*4)+(1*4)=99
99 % 10 = 9
So 7631-44-9 is a valid CAS Registry Number.

7631-44-9Upstream product

7631-44-9Downstream Products

7631-44-9Relevant academic research and scientific papers

Iron(III)Porphinate/H2O2-Mediated Conversion of All-(E)-Retinol

Waldmann, Doris,Koenig, Thorsten,Schreier, Peter

, p. 589 - 594 (2007/10/02)

The reaction of hydrogen peroxide with all-(E)-retinol (1) catalyzed by (meso-tetraphenylporphinato)iron(III) led to the formation of 4-hydroxyretinol (2), 4-oxoretinol (3), 5,8-epoxyretinol (4), 5,6-epoxyretinol (5), 3-dehydroretinol (6), all-(E)- and 12-(Z)-retroretinol (7/7a) as well as all-(E)- and 12-(Z)-anhydroretinol (8/8a) as major non-volatile products.The conversion products were characterized by comparison of their chromatographic (HPLC) and spectroscopic data (UV; MS; 1H and 13C NMR) with those of synthesized reference compounds.The observed product formation supports the hypothesis of a C4 centered radical as the key intermediate of all-(E)-retinol conversion. - Keywords: 5,6- and 5,8-Epoxyretinol, 4-Hydroxyretinol, 4-Oxoretinol, Retinol Conversion

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