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108540-96-1

4-[2-(methoxycarbonyl)anilino]-4-oxobutanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108540-96-1 Structure

  • Basic information

    1. Product Name: 4-[2-(methoxycarbonyl)anilino]-4-oxobutanoic acid
    2. Synonyms: 4-[2-(methoxycarbonyl)anilino]-4-oxobutanoic acid;3-{[2-(methoxycarbonyl)phenyl]carbamoyl}propanoic acid
    3. CAS NO:108540-96-1
    4. Molecular Formula: C12H13NO5
    5. Molecular Weight: 251.23532
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108540-96-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-[2-(methoxycarbonyl)anilino]-4-oxobutanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[2-(methoxycarbonyl)anilino]-4-oxobutanoic acid(108540-96-1)
    11. EPA Substance Registry System: 4-[2-(methoxycarbonyl)anilino]-4-oxobutanoic acid(108540-96-1)

  • 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: 108540-96-1(Hazardous Substances Data)

108540-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108540-96-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,5,4 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108540-96:
(8*1)+(7*0)+(6*8)+(5*5)+(4*4)+(3*0)+(2*9)+(1*6)=121
121 % 10 = 1
So 108540-96-1 is a valid CAS Registry Number.

108540-96-1Relevant articles and documents

N-Aryl Amides as Chemical Exchange Saturation Transfer Magnetic Resonance Imaging Contrast Agents

Cai, Xuekang,Zhang, Jia,Lu, Jiaqi,Yi, Long,Han, Zheng,Zhang, Shuixing,Yang, Xing,Liu, Guanshu

supporting information, p. 11705 - 11709 (2020/08/13)

Chemical exchange saturation transfer (CEST) MRI has recently emerged as a versatile molecular imaging approach in which diamagnetic compounds can be utilized to generate an MRI signal. To expand the scope of CEST MRI applications, herein, we systematical

Coolade. A Low-Foaming Surfactant for Organic Synthesis in Water

Lee, Nicholas R.,Cortes-Clerget, Margery,Wood, Alex B.,Lippincott, Daniel J.,Pang, Haobo,Moghadam, Farbod A.,Gallou, Fabrice,Lipshutz, Bruce H.

, p. 3159 - 3165 (2019/04/26)

Several types of reduction reactions in organic synthesis are performed under aqueous micellar-catalysis conditions (in water at ambient temperature), which produce a significant volume of foam owing to the combination of the surfactant and the presence of gas evolution. The newly engineered surfactant “Coolade” minimizes this important technical issue owing to its low-foaming properties. Coolade is the latest in a series of designer surfactants specifically tailored to enable organic synthesis in water. This study reports the synthesis of this new surfactant along with its applications to gas-involving reactions.

Radical-mediated dehydrative preparation of cyclic imides using (NH4)2S2O8-DMSO: Application to the synthesis of vernakalant

Garad, Dnyaneshwar N.,Tanpure, Subhash D.,Mhaske, Santosh B.

supporting information, p. 1008 - 1016 (2015/08/18)

Ammonium persulfate-dimethyl sulfoxide (APS-DMSO) has been developed as an efficient and new dehydrating reagent for a convenient one-pot process for the synthesis of miscellaneous cyclic imides in high yields starting from readily available primary amines and cyclic anhydrides. A plausible radical mechanism involving DMSO has been proposed. The application of this facile one-pot imide forming process has been demonstrated for a practical synthesis of vernakalant.

Reactions of Cyclic Anhydrides: Part XIII - Facile Synthesis of 1,2,3,4-Tetrahydro-10H-pyridazinoquinazoline-2,10-diones

Balasubramaniyan, V.,Argade, N. P.

, p. 906 - 908 (2007/10/02)

1,2,3,4-Tetrahydro-10H-pyridazinoquinazoline-2,10-diones have been prepared by hydrazinolysis of o-alkoxycarbonylsuccinanilic acids (IIIa-d), alkyl o-alkoxycarbonylsuccinanilates (IVa-f) or alkyl β-(4-oxo-3,1-benzoxazin-2-yl)propionates (Va,b) via

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