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4,5-dihydronaphtho[1,2-d][1,2,3]thiadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73424-56-3

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73424-56-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73424-56-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,2 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73424-56:
(7*7)+(6*3)+(5*4)+(4*2)+(3*4)+(2*5)+(1*6)=123
123 % 10 = 3
So 73424-56-3 is a valid CAS Registry Number.

73424-56-3Downstream Products

73424-56-3Relevant academic research and scientific papers

Synthesis and in vitro antifungal and cytotoxicity evaluation of substituted 4,5-dihydronaphtho[1,2-d][1,2,3]thia(or selena)diazoles.

Jalilian,Sattari,Bineshmarvasti,Daneshtalab,Shafiee, Abbas

, p. 63 - 68 (2003)

Unsubstituted 4,5-dihydronaphtho[1,2-d][1,2,3]thia (or selena)diazoles (2a, 2b), prepared from the semicarbazone (1a), were nitrated using fuming nitric acid at 0 degrees C to yield various mono-nitrated dihydronaphthalenes (3a-3e). Related sulfamoyl deri

Reaction of Substituted Hydrazones with Thionyl Chloride and Sulfuryl Chloride

Meier, Herbert,Trickes, Georg,Laping, Elisabeth,Merkle, Ursula

, p. 183 - 192 (2007/10/02)

Treatment of acetylhydrazones 2, ethoxycarbonylhydrazones 3, p-tolylsulfonylhydrazones 4 or semicarbazones 5 with thionyl chloride leads to the 1,2,3-thiadiazoles 6a-o.Sulfuryl chloride on the other hand accomplishes the transfer of chlorine without incorporating a sulfur atom.The new synthesized 1,2,3-thiadiazoles 6g-o are characterized in detail by spectroscopic methods.

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