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98876-05-2

5-(benzylamino)-4-(benzylcarbamoyl)-1-methylimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 98876-05-2 Structure

  • Basic information

    1. Product Name: 5-(benzylamino)-4-(benzylcarbamoyl)-1-methylimidazole
    2. Synonyms:
    3. CAS NO:98876-05-2
    4. Molecular Formula:
    5. Molecular Weight: 320.394
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 98876-05-2.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: 5-(benzylamino)-4-(benzylcarbamoyl)-1-methylimidazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(benzylamino)-4-(benzylcarbamoyl)-1-methylimidazole(98876-05-2)
    11. EPA Substance Registry System: 5-(benzylamino)-4-(benzylcarbamoyl)-1-methylimidazole(98876-05-2)

  • 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: 98876-05-2(Hazardous Substances Data)

98876-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98876-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,8,7 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 98876-05:
(7*9)+(6*8)+(5*8)+(4*7)+(3*6)+(2*0)+(1*5)=202
202 % 10 = 2
So 98876-05-2 is a valid CAS Registry Number.

98876-05-2Downstream Products

98876-05-2Relevant articles and documents

Reagents for Bioorganic Synthesis. 2. Methyl N-(Dicarboxymethyl)methanimidate

Lim, Benjamin B.,Hosmane, Ramachandra S.

, p. 5111 - 5115 (1985)

Preparation, properties, and reactions of the reagent methyl N-(dicarbomethoxymethyl)methanimidate (1) are reported.Dropwise addition of dimethyl aminomalonate to refluxing trimethyl orthoformate/TFA afforded 1.Treatment of 1 with ammonia and various primary amines gave the corresponding unsubstituted and 1-substituted 4-carbomethoxy-5-hydroxyimidazoles 7-12, either as the parent hydroxy compounds (a) or as the (alkyl)ammonium salts (b).The reaction of 1 with water and sodium hydrosulfide provided dimethyl N-formylaminomalonate (13) and dimethyl N-(thioformyl)aminomalonate (14), respectively.The reaction of 1 with excess sodium hydrosulfide resulted in the formation of methyl N-(thioformyl)aminoacetate (17).Conversions of methylammonium 4-carbomethoxy-1-methylimidazol-5-olate (8b) and benzylammonium 4-carbomethoxy-1-benzylimidazol-5-olate (9b) into 5-(benzylamino)-4-(benzylcarbamoyl)-1-methylimidazole (18) and 1-benzyl-5-(benzylamino)-4-(benzylcarbamoyl)imidazole (19), respectively, were each accomplished in a single-pot procedure, employing phenylphosphonic dichloride as the key reagent.

ON THE MECHANISM OF THE ONE-POT CONVERSION OF 4-CARBOMETHOXY-5-HYDROXYIMIDAZOLES INTO 5-AMINO-4-CARBAMOYLIMIDAZOLES

Hosmane, Ramachandra S.,Lim, Benjamin B.

, p. 2247 - 2250 (2007/10/02)

A mechanism is proposed for the one-pot conversion of the 4-carbomethoxy-5-hydroxyimidazoles into the corresponding 5-amino-4-carbamoylimidazoles.

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