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CAS

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90715-83-6

Propanoic acid, 3,3,3-trifluoro-2-[[[[(phenylmethyl)amino]carbonyl]amino]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 90715-83-6 Structure

  • Basic information

    1. Product Name: Propanoic acid, 3,3,3-trifluoro-2-[[[[(phenylmethyl)amino]carbonyl]amino]methyl]-
    2. Synonyms:
    3. CAS NO:90715-83-6
    4. Molecular Formula: C12H13F3N2O3
    5. Molecular Weight: 290.242
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90715-83-6.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: Propanoic acid, 3,3,3-trifluoro-2-[[[[(phenylmethyl)amino]carbonyl]amino]methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Propanoic acid, 3,3,3-trifluoro-2-[[[[(phenylmethyl)amino]carbonyl]amino]methyl]-(90715-83-6)
    11. EPA Substance Registry System: Propanoic acid, 3,3,3-trifluoro-2-[[[[(phenylmethyl)amino]carbonyl]amino]methyl]-(90715-83-6)

  • 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: 90715-83-6(Hazardous Substances Data)

90715-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90715-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,1 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90715-83:
(7*9)+(6*0)+(5*7)+(4*1)+(3*5)+(2*8)+(1*3)=136
136 % 10 = 6
So 90715-83-6 is a valid CAS Registry Number.

90715-83-6Downstream Products

90715-83-6Relevant articles and documents

Production of 5-perfluoroalkyldihydrouracil derivatives

-

, (2008/06/13)

A process for preparing a 5-perfluoroalkyl-dihydrouracil derivative of the general formula STR1 wherein Rf represents a perfluoroalkyl group, each of R1 and R2 represents a hydrogen atom, or an alkyl, cycloalkyl, aryl, aralkyl or heterocyclic group, and Y is an oxygen or sulfur atom, which comprises (a) reacting a compound of the general formula STR2 wherein X represents a halogen atom or hydroxyl group, with a urea derivative of the general formula STR3 provided that when X is a hydroxyl group and at least one of R1 and R2 is a hydrogen atom, said reaction is carried out in the presence of a condensing agent, or (b) cyclizing a compound of the general formula STR4 and a novel intermediate compound of the above formula (IV).

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