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Benzeneacetonitrile, a-[2-(dimethylamino)propyl]-a-phenyl, (R)-, also known as (R)-α-phenylbenzeneacetonitrile or (R)-α-phenylbenzyl cyanide, is a chiral organic compound with the molecular formula C15H16N. It is a derivative of benzeneacetonitrile, featuring a phenyl group attached to a cyano group and a chiral center at the α-position, which is substituted with a 2-(dimethylamino)propyl group. Benzeneacetonitrile, a-[2-(dimethylamino)propyl]-a-phenyl-, (R)- is of interest in the field of organic chemistry, particularly in the synthesis of pharmaceuticals and other specialty chemicals, due to its unique structure and potential applications in asymmetric synthesis.

7576-16-1

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7576-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7576-16-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,7 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7576-16:
(6*7)+(5*5)+(4*7)+(3*6)+(2*1)+(1*6)=121
121 % 10 = 1
So 7576-16-1 is a valid CAS Registry Number.

7576-16-1Relevant academic research and scientific papers

SYNTHESIS OF LEVOMETHADONE HYDROCHLORIDE OR DEXTROMETHADONE HYDROCHLORIDE AND METHODS FOR USE THEREOF

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Paragraph 00339-00344, (2017/03/14)

Highly efficient methods for synthesis of levomethadone hydrochloride or dextromethadone hydrochloride are provided starting from D-alanine, or L-alanine, respectively, with retention of configuration. Methods for treating a subject are provided comprising administering a composition comprising an effective amount of levomethadone hydrochloride having not more than 10 ppm dextromethadone.

Synthesis of optically active methadones, LAAM and bufuralol by lipase-catalysed acylations

Hull, Jonathan D.,Scheinmann, Feodor,Turner, Nicholas J.

, p. 567 - 576 (2007/10/03)

(R)- and (S)-Methadones and levo-α-acetylmethadol (LAAM) have been synthesised starting from lipase-catalysed acylation of dimethylaminopropan-2-ol. An approach to the synthesis of (R)-bufuralol is also presented.

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