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N-methyl-2-chloro-2-phenylethanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78899-96-4

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78899-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78899-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,9 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78899-96:
(7*7)+(6*8)+(5*8)+(4*9)+(3*9)+(2*9)+(1*6)=224
224 % 10 = 4
So 78899-96-4 is a valid CAS Registry Number.

78899-96-4Downstream Products

78899-96-4Relevant articles and documents

A General and Simple Synthesis of α-Halo Amides via α,α-Dicyano Epoxides

Pironnec, Marie-Gabrielle Le,Guinamant, Jean-Luc,Robert, Albert,Baudy-Floc'h, Michele

, p. 229 - 232 (2007/10/03)

A one-pot reaction of α,α-dicyano epoxides with amine hydrohalides provides an attractive and general route to α-halo amides.A wide variety of amines (primary alkyl, aryl, amino esters, amino amides) and epoxides (monosubstituted alkyl, aryl: disubstitute

Base-Promoted Reaction of O-Sulfonylated Hydroxamic Acids with Nucleophiles. A New Mehtod for the Synthesis of α-Substituted Amides

Hoffman, Ribert V.,Nayyar, Naresh K.,Chen, Wenting

, p. 5700 - 5707 (2007/10/02)

Treatment of a series of hydroxamic acids 2 with mesyl chloride in the presence of 2 equiv of triethylamine at 0 deg C gives 2-chloroamides 3 in good yields.Use of a single equivalent of triethylamine gives the N-(mesyloxy)amides 1, which are versatile sy

Opening of gem dicyano epoxides with amino hydrohalides: Application to the synthesis of structural analogs of tetramisole and biological evaluation

Jaguelin,Robert,Genetet,Gayral

, p. 313 - 321 (2007/10/02)

α-halogenamides are prepared in a onepot reaction by reacting gem dicyano epoxides with amino hydrohalides. This original reactivity of gem dicyano epoxides is used to prepare substituted [2,1-b]imidazothiazoles which are structural analogs of tetramisole

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