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Benzenemethanol, 2-(1-pentenyl)-, (E)-, also known as 2-(1-pentenyl)benzenemethanol or 2-(1-pentenyl)benzyl alcohol, is an organic compound with the molecular formula C12H16O. It is a chiral molecule, meaning it has a non-superimposable mirror image, and exists in two enantiomeric forms. Benzenemethanol, 2-(1-pentenyl)-, (E)- is characterized by a benzyl alcohol group (C6H5-CH2OH) and a 1-pentenyl group (CH2=CH-CH2-CH2-CH3), with the double bond in the 1-pentenyl group being in the E configuration. It is a colorless liquid with a mild, floral odor and is used in the synthesis of various pharmaceuticals, fragrances, and other organic compounds.

95330-38-4

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95330-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95330-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,3 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95330-38:
(7*9)+(6*5)+(5*3)+(4*3)+(3*0)+(2*3)+(1*8)=134
134 % 10 = 4
So 95330-38-4 is a valid CAS Registry Number.

95330-38-4Relevant academic research and scientific papers

Preparation of conformationally constrained α2 antagonists: The bicyclo[3.1.0]hexane approach

Bonnaud, Bernard,Funes, Philippe,Jubault, Nathalie,Vacher, Bernard

, p. 3360 - 3369 (2007/10/03)

The aim of the research was to discover antagonists at α2 receptor subtypes potentially more selective than known compounds. We focused on new, conformationally restricted analogues of atipamezole. The key step in the synthetic sequences leading to target compounds relied on a rhodium-catalyzed intramolecular cyclopropanation reaction, the outcome of which varied with the nature of the diazo styrene precursor. Thus, depending on the substitution pattern of the double bond and the electronic properties of the diazo precursors, the cyclopropanes 2 or 7, naphtalenes 8, or pyrazolines 17 were formed. The byproducts 8 and 17 originated from different, nonoverlapping mechanisms. Among the racemates synthesized, three compounds (1a, 22a, and 22b) showed increased selectivity for α2A vs. α2B and α2C receptor subtypes, and consequently were prepared in enantiomerically pure form. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.

Palladium-Assisted (Z)-(E) Isomerization of Styrenes

Giles, Robin G. F.,Son, Vanessa R. Lee,Sargent, Melvyn V.

, p. 777 - 781 (2007/10/02)

It is shown that treatment of stereoisomeric mixtures of styrenes with a catalytic amount of bis(acetonitrile)dichloropalladium(II) achieves smooth stereoisomerization of the (Z)-isomers to the (E)-isomers.

Aryl fatty acid leukotriene synthesis inhibitors

-

, (2008/06/13)

Aryl fatty acid compounds of the formula (I) STR1 wherein R1, R2, R3, X, and Y are as defined herein are novel and useful in the treatment of allergic and inflammatory disorders.

An Investigation into the Formation of Benzo- and Naphtho-pyrans by Cyclisation of ortho-Alkenyl(hydroxyalkyl)benzenes using either Cerium(IV) Ammonium Nitrate or Potassium t-Butoxide in Dimethylformamide

Giles, Robin G. F.,Green, Ivan R.,Pestana, J. Alexandre X.

, p. 2389 - 2396 (2007/10/02)

A series of ortho-alkenylbenzyl alcohols carrying methoxy substituents at appropriate positions on the aromatic ring have been synthesised.Each of these compounds has been treated separately with each of the title reagents.

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