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35804-09-2

1-(4-chlorophenyl)-2-(4-methoxyphenylamino)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 35804-09-2 Structure

  • Basic information

    1. Product Name: 1-(4-chlorophenyl)-2-(4-methoxyphenylamino)ethanone
    2. Synonyms: 1-(4-chlorophenyl)-2-(4-methoxyphenylamino)ethanone
    3. CAS NO:35804-09-2
    4. Molecular Formula:
    5. Molecular Weight: 275.735
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35804-09-2.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: 1-(4-chlorophenyl)-2-(4-methoxyphenylamino)ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-chlorophenyl)-2-(4-methoxyphenylamino)ethanone(35804-09-2)
    11. EPA Substance Registry System: 1-(4-chlorophenyl)-2-(4-methoxyphenylamino)ethanone(35804-09-2)

  • 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: 35804-09-2(Hazardous Substances Data)

35804-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35804-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,0 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35804-09:
(7*3)+(6*5)+(5*8)+(4*0)+(3*4)+(2*0)+(1*9)=112
112 % 10 = 2
So 35804-09-2 is a valid CAS Registry Number.

35804-09-2Relevant articles and documents

Sequential One-Pot Synthesis of Imidazoles and 2H-Imidazolones from β-Ketoamines, Acylating Agents and Ammonium Acetate

Jalani, Hitesh B.,Venkateswararao, Eeda,Manickam, Manoj,Jung, Sang-Hun

supporting information, p. 1966 - 1970 (2016/12/16)

An efficient, practical, straight forward, and transition metal-free three-component synthesis of diversely substituted imidazoles and 2H-imidazolones from β-ketoamines, acylating agents, and ammonium acetate has been described herein. This approach invol

Synthesis, Characterization, and Antibacterial Activity of Some Novel Substituted Imidazole Derivatives via One-pot Three-Component

Ramagiri, Raj Kumar,Thupurani, Murali Krishna,Vedula, Rajeswar Rao

, p. 1713 - 1717 (2015/11/09)

A simple and highly efficient one-pot, three-component synthesis of novel substituted imidazole derivatives has been reported by the reaction of 3-(2-bromoacetyl)-2H-chromen-2-one, ammonium thiocyanate, and phenacyl aniline in the presence of acetic acid

Synthesis, antibacterial activity and binding mode analysis of some novel 1,4-diaryl imidazole thiones

Ganguly, Swastika,Singh, Nalini,Upadhyay, Arpita

, p. 419 - 424 (2019/01/21)

A novel series of fifteen diaryl imidazole thiones 2a-o was synthesized by reacting the corresponding 1-(aryl)-2-(arylamino)-ethanones 1 with ammonium thiocyanate. The compounds have been characterized on the basis of elemental analysis and spectral data.

A rapid and direct access to symmetrical/unsymmetrical 3,4-diarylmaleimides and pyrrolin-2-ones

Pal, Manojit,Swamy, Nalivela Kumara,Hameed, P. Shahul,Padakanti, Srinivas,Yeleswarapu, Koteswar Rao

, p. 3987 - 3997 (2007/10/03)

1,8-Diazabicyclo[5.4.0]undec-7ene (DBU) facilitated the oxidative cyclization of phenacyl amide in the presence of atmospheric oxygen under environmentally friendly conditions. The reaction has been studied under various conditions and a plausible mechani

Hypervalent iodine mediated syntheses of heterocycles: One-pot facile syntheses of 1,4-diaryl-2-mercaptoimidazoles, 2-(α-anilinoacetyl)thiophenes and 1-aryl-2-mercapto-4-(2-thienyl)imidazoles from aryl/2-thienyl methyl ketones

Prakash, Om,Ranjana,Saini, Neena,Goyal, Seema,Tomar, Rajesh K.,Singh, Shiv P.

, p. 116 - 119 (2007/10/02)

Successive treatment of acetophenones (1a-e) or 2-acetylthiophene (4) with benzene, appropriate aniline and KSCN/AcOH leads to the formation of 1,4-diaryl-2-mercaptoimidazoles (3aa-3ea) or 1-aryl-2-mercapto-4-(2-thienyl)imidazoles (6a-f) respectively.This procedure also provides 2(α-anilinoacetyl)thiophenes (5a-f) in one pot from 4.

PREPARATION OF NEW THIOHYDROXAMIC ACID DERIVATIVES: SYNTHESIS OF SUBSTITUTED 1-HYDROXY-1,2-DIHYDROIMIDAZOLE-2-THIONES

Barton, Derek H. R.,Chern, Ching-Yu,Tachdjian, Catherine

, p. 793 - 806 (2007/10/02)

A general method for the synthesis of the title compounds is reported.The N-phenacylarylamines (11), prepared from the corresponding phenacyl bromides (9) and arylamines (10), give the thiono (or dithio) carbamates (12) on treatment with phenoxythionocarb

Nucleophilic Substitution Reactions of Phenacyl Benzenesulphonates with Anilines in Methanol-Acetonitrile Mixtures

Lee, Ikchoon,Shim, Chang Sub,Chung, Soo Young,Lee, Hai Whang

, p. 975 - 982 (2007/10/02)

The nucleophilic substitution reactions of phenacyl benzenesulphonates with anilines in methanol-acetonitrile have been studied.A stronger nucleophile was found to cause less bond cleavage, while a better leaving group led to less bond formation, in compl

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