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138375-99-2

2-amino-2-thiazolin-4-one-5-N-phenylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138375-99-2 Structure

  • Basic information

    1. Product Name: 2-amino-2-thiazolin-4-one-5-N-phenylacetamide
    2. Synonyms:
    3. CAS NO:138375-99-2
    4. Molecular Formula:
    5. Molecular Weight: 249.293
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138375-99-2.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: 2-amino-2-thiazolin-4-one-5-N-phenylacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-amino-2-thiazolin-4-one-5-N-phenylacetamide(138375-99-2)
    11. EPA Substance Registry System: 2-amino-2-thiazolin-4-one-5-N-phenylacetamide(138375-99-2)

  • 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: 138375-99-2(Hazardous Substances Data)

138375-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138375-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,7 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138375-99:
(8*1)+(7*3)+(6*8)+(5*3)+(4*7)+(3*5)+(2*9)+(1*9)=162
162 % 10 = 2
So 138375-99-2 is a valid CAS Registry Number.

138375-99-2Downstream Products

138375-99-2Relevant articles and documents

Efficient 2-amino-2-thiazolin-4-ones or 2-iminothiazolidin-4-ones formation from thioureas and maleimides under solvent-free conditions

Shimo, Tetsuro,Matsuda, Yuki,Iwanaga, Tetsuo,Shinmyozu, Teruo,Somekawa, Kenichi

, p. 1053 - 1058 (2007)

A facile method for the construction of 2-thiazolin-4-one or thiazolidin-4-one structure is described. Condensation reactions of thiourea (1a) and maleimides (2) under solvent-free conditions gave 2-amino-2-thiazolin-4-ones (3) via Michael-type reaction, while similar reactions of N-substituted thioureas (1b-d) with 2 afforded 2-iminothiazolidin-4-ones (4). Since the solvent-free reactions of 1 with 2a afforded 3 in good yields, the synthetic method was found to be effective from the viewpoint of green chemistry.

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