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Carbamic acid, (1-methyl-2-phenylethyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27822-59-9

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27822-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27822-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,2 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27822-59:
(7*2)+(6*7)+(5*8)+(4*2)+(3*2)+(2*5)+(1*9)=129
129 % 10 = 9
So 27822-59-9 is a valid CAS Registry Number.

27822-59-9Downstream Products

27822-59-9Relevant articles and documents

Determination of the synthetic origin of methamphetamine samples by 2H NMR spectroscopy

Armellin, Silvia,Brenna, Elisabetta,Frigoli, Samuele,Fronza, Giovanni,Fuganti, Claudio,Mussida, Daniele

, p. 3113 - 3117 (2008/02/09)

Samples of methamphetamine, prepared according to the most common synthetic pathways, were submitted to natural-abundance 2H NMR spectroscopy. The deuterium content at the various sites of the molecule was found to depend on its synthetic history. The technique provides a chemical fingerprint of methamphetamine samples and can give hints to trace back the starting materials and the synthetic procedures.

Asymmetric organic synthesis. Preparation and Birch reduction-alkylation of 2-methyl-3,4-dihydroisoquinolin-1-ones

Schultz, Arthur G.,Kirincich, Steven J.,Rahm, Rainer

, p. 4551 - 4554 (2007/10/02)

Birch reductions of 2-methyl-3,4-dihydroisoquinolin-1-ones 1 and 6 generate enolates 2a and 2b and alkylations provide 1,4-cyclohexadienes 3a-3e and 7a-7c. The synthesis of a racemic structural analogue, 9, of the potent analgetic levorphanol is described.

1-Ethoxy-3,4-dihydroisoquindines

-

, (2008/06/13)

1-(2-Substituted-hydrazino)-3,4-dihydroisoquinolines, prepared in one process by alkylating the corresponding 3,4-dihydroisocarbostyrils, hydrazinolyzing the resulting 1-alkoxy-3,4-dihydroisoquinolines and condensing the resulting 1-hydrazIno-3,4-dihydroisoquinolines with aldehydes or ketones, and 1,1'-azinobis(1,2,3,4-tetrahydroisoquinolines), prepared by condensing corresponding 1-alkoxy-3,4-dihydroisoquinolines and 1-hydrazino-3,4-dihydroisoquinolines, are useful as antihypertensive agents and/or as antiinflammatory agents.

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