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N,N-diethyl-3-methylsalicylamide methyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72003-94-2

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72003-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72003-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,0 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72003-94:
(7*7)+(6*2)+(5*0)+(4*0)+(3*3)+(2*9)+(1*4)=92
92 % 10 = 2
So 72003-94-2 is a valid CAS Registry Number.

72003-94-2Relevant articles and documents

Regiocontrolled rearrangement of isobenzofurans

Egan, Ben A.,Paradowski, Michael,Thomas, Lynne H.,Marquez, Rodolfo

, p. 2086 - 2089 (2011)

Regioselective alkylation and oxidative rearrangement of isobenzofurans has been achieved to generate substituted 4,8- ihydroxyisochromanones in good yields and with complete regiocontrol.

Regiodivergent Iodocyclizations for the Highly Diastereoselective Synthesis of syn - And anti -Hydroxyl-Isochromanones and -Isobenzofuranones: Concise Synthesis of the Isochromanone Core of the Ajudazols

Thiede, Sebastian,Winterscheid, Peter Maria,Hartmann, Jan,Schnakenburg, Gregor,Essig, Sebastian,Menche, Dirk

, p. 697 - 709 (2016/03/01)

An efficient synthetic strategy to access hydroxyl-isochromanone and -isobenzofurans from readily available joint alkene precursors by a regiodivergent one-pot iodocyclization-substitution tandem process is reported. The cyclizations proceed with excellen

Stereoselective Synthesis of Isochromanones by an Asymmetric Ortho-Lithiation Strategy: Synthetic Access to the Isochromanone Core of the Ajudazols

Essig, Sebastian,Menche, Dirk

, p. 1943 - 1966 (2016/03/15)

Full details on the design, development, and application of a highly stereoselective strategy for the synthesis of isochromanones are reported. The method is based on an asymmetric ortho lithiation with aldehyde electrophiles and utilizes the chiral memor

Beyond directed ortho metalation: Ru-catalyzed CAr-O activation/cross-coupling reaction by amide chelation

Zhao, Yigang,Snieckus, Victor

supporting information, p. 11224 - 11227 (2014/09/29)

Disclosed is a new, catalytic, and general methodology for the chemical synthesis of biaryl, heterobiaryl, and polyaryl molecules by the cross-coupling of o-methoxybenzamides with aryl boroneopentylates. The reaction is based on the activation of the unreactive C-OMe bond by the proximate amide directing group using catalytic RuH2(CO)(PPh3)3 conditions. A one-step, base-free coupling process is thereby established that has the potential to supersede the useful two-step directed ortho metalation/cross- coupling reaction involving cryogenic temperature and strong base conditions. High regioselectivity, orthogonality with the Suzuki-Miyaura reaction, operational simplicity, minimum waste, and convenient scale-up make these reactions suitable for industrial applications.

Structurally Modified Isokalafungins and Isonanaomycins

Hoffmann, Bernd,Lackner, Helmut

, p. 87 - 94 (2007/10/02)

The total synthesis of structural analogues of the unnatural, C-6-hydroxylated isokalafungins and isonanaomycins is described.The new compounds show improved antibiotic activity and support theories for a mechanism of action which base on the formation of

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