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

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  • 53979-33-2 Structure
  • Basic information

    1. Product Name: 3-(3,4-dimethoxyphenyl)-2-methylpropanoic acid
    2. Synonyms: 3-(3,4-dimethoxyphenyl)-2-methylpropanoic acid
    3. CAS NO:53979-33-2
    4. Molecular Formula:
    5. Molecular Weight: 224.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53979-33-2.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: 3-(3,4-dimethoxyphenyl)-2-methylpropanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(3,4-dimethoxyphenyl)-2-methylpropanoic acid(53979-33-2)
    11. EPA Substance Registry System: 3-(3,4-dimethoxyphenyl)-2-methylpropanoic acid(53979-33-2)
  • 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: 53979-33-2(Hazardous Substances Data)

53979-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53979-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,7 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53979-33:
(7*5)+(6*3)+(5*9)+(4*7)+(3*9)+(2*3)+(1*3)=162
162 % 10 = 2
So 53979-33-2 is a valid CAS Registry Number.

53979-33-2Relevant articles and documents

Pd-Catalyzed Regioselective Branched Hydrocarboxylation of Terminal Olefins with Formic Acid

Chu, Jianxiao,Guo, Jianqiong,Ren, Wenlong,Shi, Yian,Shi, Yuan,Wang, Mingzhou,Zhou, Jintao

supporting information, p. 886 - 891 (2022/02/07)

A regioselective Pd-catalyzed hydrocarboxylation of terminal olefins with HCOOH is described. A wide variety of branched carboxylic acids can readily be obtained with high regioselectivities under mild reaction conditions. The reaction is operationally simple and requires no handling of toxic CO. The ligand and LiCl are important factors for reaction reactivity and selectivity.

DERIVATIVES OF SULINDAC CAN PROTECT NORMAL CELLS AGAINST OXIDATIVE DAMAGE

-

Page/Page column 33; 34, (2018/10/19)

The disclosure provides chemical compounds possessing therapeutic and/or protective properties against oxidative damage. Methods of making such therapeutic and/or protective compounds and associated compositions are also provided, as are methods for their use, which include protecting cells from oxidative damage and/or inhibiting production of ROS in a cell or subject, as well as preventing or reducing the extent of tissue damage caused by an ischemic event in a subject at elevated risk of such an event.

Concise synthesis of 2-benzazepine derivatives and their biological activity

So, Masahiro,Kotake, Tomoko,Matsuura, Kenji,Inui, Makoto,Kamimura, Akio

, p. 4017 - 4028 (2012/06/15)

Figure Persented: 2-Benzazepines, which are potentially good candidates for new drug therapies to treat skin wounds, were readily prepared from substituted cinnamylamide via an intramolecular Friedel-Crafts reaction. With few steps and effective reactions

Probing the steric space at the floor of the D1 dopamine receptor orthosteric binding domain: 7α-, 7β-, 8α-, and 8β-methyl substituted dihydrexidine analogues

Cueva, Juan Pablo,Gallardo-Godoy, Alejandra,Juncosa, Jose I.,Vidi, Pierre A.,Lill, Markus A.,Watts, Val J.,Nichols, David E.

, p. 5508 - 5521 (2011/10/02)

To probe the space at the floor of the orthosteric ligand binding site in the dopamine D1 receptor, four methylated analogues of dihydrexidine (DHX) were synthesized with substitutions at the 7 and 8 positions. The 8α-axial, 8β-equatorial, and

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