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ethyl (Z)-2-benzoylamino-3-(indol-3-yl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79722-90-0

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79722-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79722-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,2 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79722-90:
(7*7)+(6*9)+(5*7)+(4*2)+(3*2)+(2*9)+(1*0)=170
170 % 10 = 0
So 79722-90-0 is a valid CAS Registry Number.

79722-90-0Downstream Products

79722-90-0Relevant articles and documents

Reaction of imidazole and indole with 4-ethoxyalkylidene-2-phenyl-2-oxazolin-5-one: Structure of the condensation products

Homami, Seyed-Saied,Mukerjee, Arya K.

, p. 359 - 361 (2007/10/02)

Imidazole (2) and indole (3a) react with 4-ethoxymethylene-2-phenyl-2-oxazolin-5-one (1b; R2=H) to give 4-(imidazol-1-ylmethylene)- and 4-skatylidene-2-phenyl-2-oxazolin-5-ones (1d and 1e), respectively.Their structure are discussed.

TRIETHYLAMINE, ETHANOL- MEDIATED DISCIPLINED REACTIONS OF S-BENZYLISOTHIOURONIUM CHLORIDE WITH UNSATURATED 2-OXAZOLIN-5-ONES: SYNTHESIS OF (Z)-2-AMINO-4-ARYLMETHYLENE-2-IMIDAZOLIN-5-ONES, 5-BENZOYLAMINO-2-BENZYLTHIO-6-OXO-4,4-SPIROCYCLOHEXYL-1,4,5,6-TETRA

Mukerjee, Arya K.,Joseph, Kiran,Homami, Seyed-Saied,Tikdari, Ahmad M.

, p. 1317 - 1325 (2007/10/02)

Triethylamine-mediated condensation of S-benzylisothiouronium chloride with (Z)-4-arylmethylene-2-phenyl-2-oxazolin-5-ones (4) in ethanol gives (Z)-2-amino-4-arylmethylene-2-imidazolin-5-ones (7), whereas the similar reaction with 4-cyclohexylidene-2-phen

Useful Synthesis of α,β-Dehydrotryptophan Derivatives

Moriya, Tamon,Yoneda, Naoto,Miyoshi, Muneji,Matsumoto, Kazuo

, p. 94 - 98 (2007/10/02)

N-Acyl-α,β-dehydrotryptophan (ΔTrp) esters 4a-h were directly synthesized by the reaction of 3--3H-indole (2) with N-acylglycinates 3a-h in resonable yields.Of these, N-formyl-substituted ΔTrp methyl ester (4a) was easily converted into ΔTrp methyl ester (7) in a high yield by acidolysis with dry methanol-hydrogen chloride.Furthermore, 7 was successfully used for the preparation of a dipeptide, N-alanyl-substituted ΔTrp methyl ester (10).

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