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(2S,4aR,8R,8aR)-4a,5,8,8a-tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4,4,7-trimethyl-4H-1,3-benzodioxin-8-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1292847-79-0

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1292847-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1292847-79-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,2,8,4 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1292847-79:
(9*1)+(8*2)+(7*9)+(6*2)+(5*8)+(4*4)+(3*7)+(2*7)+(1*9)=200
200 % 10 = 0
So 1292847-79-0 is a valid CAS Registry Number.

1292847-79-0Downstream Products

1292847-79-0Relevant academic research and scientific papers

Transformations of several monoterpenoids in the presence of aldehydes in supercritical solvents

Anikeev,Sivcev,Il'Ina,Korchagina,Statsenko,Volcho,Salakhutdinov

, p. 382 - 387 (2013/07/26)

The reactivity of verbenol epoxide and isopulegol in supercritical solvents in the presence of aromatic aldehydes was studied using a flow type reactor and a heterogeneous catalyst (Al2O3) or no catalyst. The intramolecular transformations or interactions of reagents with the solvent prevailed in all cases; the yield of the products of intermolecular reactions of terpenoids with aldehydes was up to 1%. The aldehydes did not interact with verbenol epoxide but produced a considerable effect on the distribution of its isomerization products.

Reactions of verbenol epoxide with aromatic aldehydes containing hydroxy or methoxy groups in the presence of montmorillonite clay

Il'ina, Irina V.,Volcho, Konstantin P.,Mikhalchenko, Oksana S.,Korchagina, Dina V.,Salakhutdinov, Nariman F.

experimental part, p. 502 - 513 (2011/04/25)

The reactions of (-)-cis-verbenol epoxide with a number of aromatic aldehydes containing OH and/or MeO groups in the presence of montmorillonite K10 clay have been studied. Several new O-containing heterocyclic compounds with different frameworks, including compounds with a previously unknown octahydro-2H-4,6-(epoxymethano)chromene framework, have been synthesized. Introduction of one donor substituent in the benzaldehyde molecule led to a decrease in the total yield of intermolecular by formed products, while the introduction of two and more substituents led to an increase in the yield of these products.

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