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ethyl 2-(2,4-dimethylphenyl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105337-16-4 Structure
  • Basic information

    1. Product Name: ethyl 2-(2,4-dimethylphenyl)acetate
    2. Synonyms: ethyl 2-(2,4-dimethylphenyl)acetate
    3. CAS NO:105337-16-4
    4. Molecular Formula:
    5. Molecular Weight: 192.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105337-16-4.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: ethyl 2-(2,4-dimethylphenyl)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-(2,4-dimethylphenyl)acetate(105337-16-4)
    11. EPA Substance Registry System: ethyl 2-(2,4-dimethylphenyl)acetate(105337-16-4)
  • 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: 105337-16-4(Hazardous Substances Data)

105337-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105337-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,3 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 105337-16:
(8*1)+(7*0)+(6*5)+(5*3)+(4*3)+(3*7)+(2*1)+(1*6)=94
94 % 10 = 4
So 105337-16-4 is a valid CAS Registry Number.

105337-16-4Relevant articles and documents

Reductive removal of phenylseleno groups from α-phenylseleno carbonyl compounds by means of tellurolate anions

Silveira,Lenardao,Comasseto

, p. 575 - 582 (1994)

α-Phenylseleno carbonyl compounds are reduced to the corresponding selenium free carbonyl compounds by reaction with organic and inorganic tellurolate anions.

Palladium-catalyzed cross-coupling of sterically demanding boronic acids with α-bromocarbonyl compounds

Zimmermann, Bettina,Dzik, Wojciech I.,Himmler, Thomas,Goossen, Lukas J.

experimental part, p. 8107 - 8112 (2011/11/07)

A catalyst system generated in situ from Pd(dba)2 and tri(o-tolyl)phosphine mediates the coupling of arylboronic acids with alkyl α-bromoacetates under formation of arylacetic acid esters at unprecedented low loadings. The new protocol, which involves potassium fluoride as the base and catalytic amounts of benzyltriethylammonium bromideas a phase transfer catalyst, is uniquely effective for the synthesis of sterically demanding arylacetic acid derivatives. (Figure presented)

6-Substituted pyridoindolone derivatives, production and therapeutic use thereof

-

Page/Page column 12; 13, (2010/11/27)

Compounds of formula: and pharmaceutically acceptable salts, hydrates, and solvates thereof, wherein R1, R2, R3, R4, and R5, have the meanings given in the description; pharmaceutical compositions comprising said compounds; and processes for preparing said compounds and methods of use thereof.

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