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CAS

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1338698-47-7

1-(2-aminophenyl)-4,4-dimethylpent-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1338698-47-7 Structure

  • Basic information

    1. Product Name: 1-(2-aminophenyl)-4,4-dimethylpent-2-en-1-one
    2. Synonyms: 1-(2-aminophenyl)-4,4-dimethylpent-2-en-1-one
    3. CAS NO:1338698-47-7
    4. Molecular Formula:
    5. Molecular Weight: 203.284
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1338698-47-7.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-(2-aminophenyl)-4,4-dimethylpent-2-en-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-aminophenyl)-4,4-dimethylpent-2-en-1-one(1338698-47-7)
    11. EPA Substance Registry System: 1-(2-aminophenyl)-4,4-dimethylpent-2-en-1-one(1338698-47-7)

  • 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: 1338698-47-7(Hazardous Substances Data)

1338698-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338698-47-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,6,9 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1338698-47:
(9*1)+(8*3)+(7*3)+(6*8)+(5*6)+(4*9)+(3*8)+(2*4)+(1*7)=207
207 % 10 = 7
So 1338698-47-7 is a valid CAS Registry Number.

1338698-47-7Relevant articles and documents

An efficient one-step synthesis of 2-arylquinolin-4(1H)-ones with the aid of a low-valent titanium reagent

Sun, Fang,Zhao, Xuan,Shi, Daqing

, p. 5633 - 5635 (2011)

A short and facile synthesis of a series of 2-arylquinolin-4(1H)-ones was accomplished in good yields via the novel reductive cyclization of 2-nitrochalcones promoted by TiCl4/Zn. This method has the advantages of accessible starting materials,

A Convenient Formal [4+2] Heterocylization Route to Bis(triflyl)tetrahydroquinolines

Lázaro-Milla, Carlos,Almendros, Pedro

, p. 13534 - 13538 (2021/08/13)

We report the sustainable and efficient synthesis of a new type of quinoline derivatives bearing one or two SO2CF3 groups. The protocol is metal-, catalyst- and irradiation-free, involves the use of readily available and stable precursors, and avoids the formation of side products. Also, the mild conditions of the process allow the tolerance of a wide range of functional groups.

Chiral Phosphoric Acid Catalyzed Asymmetric Synthesis of 2-Substituted 2,3-Dihydro-4-quinolones by a Protecting-Group-Free Approach

Saito, Kodai,Moriya, Yuka,Akiyama, Takahiko

supporting information, p. 3202 - 3205 (2015/07/15)

Chiral 2-substituted 2,3-dihydro-4-quinolones were synthesized based on the chiral phosphoric acid catalyzed intramolecular aza-Michael addition reaction using N-unprotected 2-aminophenyl vinyl ketones as substrates in good yields with high enantioselectivities. (Chemical Equation Presented).

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