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125610-66-4

diethyl β-anilinobenzylidenemalonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125610-66-4 Structure

  • Basic information

    1. Product Name: diethyl β-anilinobenzylidenemalonate
    2. Synonyms: diethyl β-anilinobenzylidenemalonate
    3. CAS NO:125610-66-4
    4. Molecular Formula:
    5. Molecular Weight: 339.391
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125610-66-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: diethyl β-anilinobenzylidenemalonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl β-anilinobenzylidenemalonate(125610-66-4)
    11. EPA Substance Registry System: diethyl β-anilinobenzylidenemalonate(125610-66-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 125610-66-4(Hazardous Substances Data)

125610-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125610-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,6,1 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125610-66:
(8*1)+(7*2)+(6*5)+(5*6)+(4*1)+(3*0)+(2*6)+(1*6)=104
104 % 10 = 4
So 125610-66-4 is a valid CAS Registry Number.

125610-66-4Relevant articles and documents

Iodine-mediated synthesis of 3 H -indoles via intramolecular cyclization of enamines

He, Zhiheng,Li, Huanrong,Li, Zhiping

supporting information; experimental part, p. 4636 - 4639 (2010/09/15)

(Figure presented) The synthesis of 3H-indoles was achieved via the iodine-mediated intramolecular cyclization of enamines. A wide variety of 3H-indole derivatives bearing multifunctional groups were obtained in good to high yields under transition metal-free reaction conditions.

2-Aryl-4-quinolones and Fused Quinolines from β-Chloroarylidenemalonates and Related Chloro Esters

Hormi, Osmo E.,Peltonen, Carita,Heikkilae, Laila

, p. 2513 - 2515 (2007/10/02)

The β-chloroarylidenemalonates I were transformed to the anilinoarylidenemalonates II in 50-70 percent yield.Thermolysis of th β-anilinofurfurylidenemalonate IIc at 250 deg C gave 3-(ethoxycarbonyl)-2-(2-furyl)-4-quinolone III in 85percent yield.Treatment

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