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110577-68-9

2-(4-chlorobenzyl)-3,3-dimethylbutanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 110577-68-9 Structure

  • Basic information

    1. Product Name: 2-(4-chlorobenzyl)-3,3-dimethylbutanoic acid
    2. Synonyms:
    3. CAS NO:110577-68-9
    4. Molecular Formula: C13H17ClO2
    5. Molecular Weight: 240.7259
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 110577-68-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 342.9°C at 760 mmHg
    3. Flash Point: 161.2°C
    4. Appearance: N/A
    5. Density: 1.136g/cm3
    6. Vapor Pressure: 2.79E-05mmHg at 25°C
    7. Refractive Index: 1.529
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(4-chlorobenzyl)-3,3-dimethylbutanoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(4-chlorobenzyl)-3,3-dimethylbutanoic acid(110577-68-9)
    12. EPA Substance Registry System: 2-(4-chlorobenzyl)-3,3-dimethylbutanoic acid(110577-68-9)

  • 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: 110577-68-9(Hazardous Substances Data)

110577-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110577-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,7 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 110577-68:
(8*1)+(7*1)+(6*0)+(5*5)+(4*7)+(3*7)+(2*6)+(1*8)=109
109 % 10 = 9
So 110577-68-9 is a valid CAS Registry Number.

110577-68-9Relevant articles and documents

On the mechanism of the addition of organolithium reagents to cinnamic acids

Aurell, María José,Ba?uls, María José,Mestres, Ramon,Mu?oz, Elena

, p. 1067 - 1074 (2007/10/03)

The regioselectivity of the addition of tert-butyllithium to cinnamic acid is subject to reaction conditions and to substituent electronic effects. Significant effects are observed in the presence of several additives including a radical trap such as α-methylstyrene. Competition experiments by addition of the organolithium reagent to mixtures of substituted cinnamic acids show that the relative rates of both conversion of the starting acids and formation of the 1,3-adducts are subject to electronic effects, whereas rates for 1,4-addition are independent of the substituents. These features are in agreement with a polar addition mechanism, but a fast SET equilibrium followed by slow radical combination would be possible as well.

Structure-Activity Relationships in Fungicidal 1-(2-Benzyl-3,3-dimethylbutanoyl)imidazoles and Related Compounds

Manabe, Akio,Kirino, Osamu,Furuzawa, Kunihiko,Takano, Hirotaka,Hisada, Yoshio,Tanaka, Shizuya

, p. 1959 - 1966 (2007/10/02)

1-(2-Benzyl-3,3-dimethylbutanoyl)imidazoles and related compounds were prepared and tested for their fungicidal activity against powdery mildew on barley (Erysiphe graminis) and gray mold on cucumber (Botrytis cinerea) by pot tests.The benzyl group at the

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