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2-(ethoxycarbonyl)amino-3-(2'-phenylethynyl)naphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107784-18-9

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107784-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107784-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,7,8 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 107784-18:
(8*1)+(7*0)+(6*7)+(5*7)+(4*8)+(3*4)+(2*1)+(1*8)=139
139 % 10 = 9
So 107784-18-9 is a valid CAS Registry Number.

107784-18-9Downstream Products

107784-18-9Relevant academic research and scientific papers

Method of colorimetric analysis of malonic dialdehyde and 4-hydroxy-2-enaldehydes as indexes of lipid peroxidation, kits for carrying out said method, substituted indoles for use in said method and their preparation

-

, (2008/06/13)

A colorimetric assay of enaldehydes or of malonic dialdehyde as lipid peroxidation indices in an aqueous medium including a) addition to the medium of a reagent of a compound of general formula I and their optional addition salts with organic or inorganic bases or with organic or inorganic acids. STR1 in which formula: A and C, which may be identical or different, each represent H, STR2 wherein A and C cannot simultaneously represent H, with: R1 =H; alkyl; aralkyl; aryl substituted on the aryl ring; alkyl sulfonate Y+ ; alkyl phosphonate, Y+ ; or alkyl carboxylate, Y+ ; R2 =H; --OR4 ; F; Cl; Br; I; --NO2 ; SO331 Y+ ; --CN; --COOR4 ; or --CONR5 R6 ; R3 =H; --OR4 ; --NR5 R6 ; --SR4 ; F; Cl; Br; I; --NO2 ; --SO3 --Y+ ; --CN; --COR5 ; --COOR4 ; or --CONR5 R6 ; R4 =H; alkyl; aralkyl; or aryl substituted on the aryl ring; R5 =H; alkyl; aralkyl; or aryl substituted on the aryl ring; R6 =H; aryl, aralkyl; or aryl substituted on the aryl ring; Y+ =cation of an organic or inorganic base; STR3 wherein alkyl represents a linear or branched group comprising 1 to 6 carbon; aryl is substituted on the aryl ring with one or more groups which may be identical or different selected from C1-6 alkyl, alkoxy, hydroxy, amino and carboxyl; b) acidification of the medium; and c) incubation of the acidified medium. Requisites or kits for the implementation of the process are also disclosed.

CONDENSED HETEROAROMATIC SYSTEMS. X. SYNTHESIS OF BENZINDOLES FROM o-BROMONAPHTHYLAMINES

Sakamoto, Takao,Kondo, Yoshinori,Yamanaka, Hiroshi

, p. 1845 - 1847 (2007/10/02)

benzindole, of which few effective preparative methods are known, was easily synthesized by palladium-catalyzed reaction of ethyl 3-bromo-2-naphthylcarbamate with trimethylsilylacetylene and subsequent cyclization with sodium ethoxide in ethanol.By the same method , benzindole and benzindole were obtained from 2-bromo-1-naphthylcarbamate and 1-bromo-2-naphthylcarbamate, respectively.

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