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Benzenemethanol, a-butyl-2-hydroxy-3-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92759-34-7

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92759-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92759-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,7,5 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92759-34:
(7*9)+(6*2)+(5*7)+(4*5)+(3*9)+(2*3)+(1*4)=167
167 % 10 = 7
So 92759-34-7 is a valid CAS Registry Number.

92759-34-7Relevant academic research and scientific papers

Isolation, Synthesis, Structure-Activity Relationships of Bioactive Benzoquinones from Miconia lepidota from the Suriname Rainforest

Gunatilaka, A. A. Leslie,Berger, John M.,Evans, Randy,Miller, James S.,Wisse, Jan H.,Neddermann, Kim M.,Bursuker, Isia,Kingston, David G. I.

, p. 2 - 5 (2007/10/03)

Bioactivity-directed fractionation of an EtOAc extract from the leaves of Miconia lepidota afforded the two benzoquinones 2-methoxy-6-heptyl-1,4-benzoquinone (1) and 2-methoxy-6-pentyl-1,4-benzoquinone (primin) (2). This is the first reported isolation of

Synthesis of Side-Chain-Modified Analogues of the Allergen Primin

Koenig, Wilfried A.,Faasch, Holger,Heitsch, Holger,Colberg, Cornelia,Hausen, Bjoern M.

, p. 387 - 393 (2007/10/02)

Benzoquinones such as primin (2-methoxy-6-pentyl-1,4-benzoquinone) from Primula obconica HANCE (Primulaceae) are known to be strong sensitizers and thus the source of severe allergic contact dermatitis (cell-mediated type of allergy).In order to determine

Ortho Lithiation of 2-Hydroxymethyl-1,4,5,6,8-pentamethoxynaphthalene, a Supplement

Tanoue, Yasuhiro,Terada, Akira

, p. 2295 - 2297 (2007/10/02)

The structures of the products in our previous report "One-Pot Hydroxylations of 2-(1-Hydroxyalkyl)naphthalenes and (1-Hydroxyalkyl)benzenes" were reexamined by 13C NMR spectra and part of our previous interpretation will be corrected here.The lithiations of 2-(1-hydroxyalkyl)-1,4,5,6,8-pentamethoxynaphthalenes occurred at the 7-position, and not at the 3-position as were reported.

One-Pot Ortho Hydroxylation of 2-(1-Hydroxyalkyl)naphthalenes and (1-Hydroxyalkyl)benzenes

Tanoue, Yasuhiro,Terada, Akira,Seto, Iwao,Umezu, Yasuo,Tsuge, Otohiko

, p. 1221 - 1224 (2007/10/02)

Hydroxylations of 2-(1-hydroxyalkyl)-1,4,5,8(or 1,4,5,6,8)-tetra(or penta)methoxynaphthalenes and 2-(1-hydroxyalkyl)-1,4-dimethoxybenzenes at the 3-position were accomplished by a one-spot procedure.The same procedure has been found to be applicable to 2-(1-hydroxyalkyl)naphthalenes and (1-hydroxyalkyl)benzenes having no methoxy substituent.

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