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108087-86-1

4-(4-butoxyanilino)-4-oxo-2-butenoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108087-86-1 Structure

  • Basic information

    1. Product Name: 4-(4-butoxyanilino)-4-oxo-2-butenoic acid
    2. Synonyms: 4-(4-butoxyanilino)-4-oxo-2-butenoic acid
    3. CAS NO:108087-86-1
    4. Molecular Formula: C14H17NO4
    5. Molecular Weight: 263.28908
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108087-86-1.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-(4-butoxyanilino)-4-oxo-2-butenoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-butoxyanilino)-4-oxo-2-butenoic acid(108087-86-1)
    11. EPA Substance Registry System: 4-(4-butoxyanilino)-4-oxo-2-butenoic acid(108087-86-1)

  • 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: 108087-86-1(Hazardous Substances Data)

108087-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108087-86-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,0,8 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108087-86:
(8*1)+(7*0)+(6*8)+(5*0)+(4*8)+(3*7)+(2*8)+(1*6)=131
131 % 10 = 1
So 108087-86-1 is a valid CAS Registry Number.

108087-86-1Relevant articles and documents

Synthesis of N-butoxyphenylmaleimides

Kolyamshin,Vasil'eva,Kol'tsov

, p. 1614 - 1615 (2007/10/03)

Reactions of equimolar amounts of o-, m-, and p-butoxyanilines with maleic anhydride give the corresponding N-butoxyphenylmaleamic acids which undergo cyclization into N-butoxyphenylmaleimides by the action of acetic anhydride in dimethylformamide in the presence of sodium acetate.

Synthesis of N-Aryl/heteroaryl/-substituted-methyl-&α-(p-substituted anilino)succinimides as Antituberculosis Agents

Rangnekar, V. M.,Bhamaria, R. P.,Khadse, B. G.

, p. 342 - 344 (2007/10/02)

A series of N-Aryl/heteroaryl/substituted-methyl-α-(p-substituted anilino)succinimides (II) have been prepared and screened in vitro against H37Rv strain of Mycobacterium tuberculosis.Some of these compounds exhibit activity upto 0.39 μg/ml concentration.

Synthesis of N-Aryl/substituted-methyl/heteroaryl-&α-pyrrolidino/piperidino Succinimides as Antituberculosis Agents

Rangnekar, V. M.,Lokhande, S. R.,Bhamaria, R. P.,Khadse, B. G.

, p. 1070 - 1071 (2007/10/02)

A series of N-Aryl/substituted-methyl/heteroaryl-α-pyrrolidino- and piperidino-succinimides (II) have been prepared and screened in vitro against H37Rv strain of Mycobacterium tuberculosis.Some of these compounds exhibit activity upto 1.56 μg/ml concentration.

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