Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1245919-59-8

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

1245919-59-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1245919-59-8 Structure

  • Basic information

    1. Product Name: methyl 2-(2,4-dimethylphenyl)-2-oxoethanoate
    2. Synonyms: methyl 2-(2,4-dimethylphenyl)-2-oxoethanoate
    3. CAS NO:1245919-59-8
    4. Molecular Formula:
    5. Molecular Weight: 192.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1245919-59-8.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: methyl 2-(2,4-dimethylphenyl)-2-oxoethanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-(2,4-dimethylphenyl)-2-oxoethanoate(1245919-59-8)
    11. EPA Substance Registry System: methyl 2-(2,4-dimethylphenyl)-2-oxoethanoate(1245919-59-8)

  • 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: 1245919-59-8(Hazardous Substances Data)

1245919-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1245919-59-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,9,1 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1245919-59:
(9*1)+(8*2)+(7*4)+(6*5)+(5*9)+(4*1)+(3*9)+(2*5)+(1*9)=178
178 % 10 = 8
So 1245919-59-8 is a valid CAS Registry Number.

1245919-59-8Relevant articles and documents

Electrochemical synthesis of the aryl α-ketoesters from acetophenones mediated by Ki

Zhang, Zhenlei,Su, Jihu,Zha, Zhenggen,Wang, Zhiyong

, p. 17711 - 17714 (2013)

Two C-O bonds formed in one step: The oxidative coupling reaction of acetophenones with alcohol was developed by a dioxygen activation to afford α-ketoesters under electrochemical conditions. This novel transformation not only provides a simple and efficient approach to synthetize α-ketoester derivatives, but also invents a new strategy to construct a C-O bond by virtue of an anode oxidation (see scheme). Copyright

Rh-catalyzed asymmetric hydrogenation of racemic aldimines via dynamic kinetic resolution

Fan, Dongyang,Lu, Jian,Liu, Yang,Zhang, Zhenfeng,Liu, Yangang,Zhang, Wanbin

, p. 5541 - 5547 (2016/08/05)

Catalyzed by a rhodium complex of P-stereogenic diphosphine ligand trichickenfootphos (TCFP), asymmetric hydrogenation of racemic aldimines via dynamic kinetic resolution has been realized for the preparation of chiral arylglycines with good yields and enantioselectivities.

Palladium-catalyzed [4 + 2] cycloaddition of o-(silylmethyl)benzyl esters with ketones: An equivalent to oxo-diels-alder reaction of o-xylylenes

Ueno, Satoshi,Ohtsubo, Masakazu,Kuwano, Ryoichi

supporting information; experimental part, p. 4332 - 4334 (2010/12/19)

Figure Presented. o-(Silylmethyl)benzyl carbonates reacted with various electron-deficient ketones in the presence of a palladium catalyst, affording the [4 + 2] cycloaddition products, isochromanes, in high yields. The palladium-catalyzed cycloaddition i

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1245919-59-8