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CAS

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1332827-99-2

(S)-2,2,2-trifluoro-N-(1-(2-(trifluoromethyl)phenyl)ethyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1332827-99-2 Structure

  • Basic information

    1. Product Name: (S)-2,2,2-trifluoro-N-(1-(2-(trifluoromethyl)phenyl)ethyl)acetamide
    2. Synonyms:
    3. CAS NO:1332827-99-2
    4. Molecular Formula:
    5. Molecular Weight: 285.189
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1332827-99-2.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: (S)-2,2,2-trifluoro-N-(1-(2-(trifluoromethyl)phenyl)ethyl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2,2,2-trifluoro-N-(1-(2-(trifluoromethyl)phenyl)ethyl)acetamide(1332827-99-2)
    11. EPA Substance Registry System: (S)-2,2,2-trifluoro-N-(1-(2-(trifluoromethyl)phenyl)ethyl)acetamide(1332827-99-2)

  • 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: 1332827-99-2(Hazardous Substances Data)

1332827-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1332827-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,8,2 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1332827-99:
(9*1)+(8*3)+(7*3)+(6*2)+(5*8)+(4*2)+(3*7)+(2*9)+(1*9)=162
162 % 10 = 2
So 1332827-99-2 is a valid CAS Registry Number.

1332827-99-2Downstream Products

1332827-99-2Relevant articles and documents

Sequential reductive amination-hydrogenolysis: A one-pot synthesis of challenging chiral primary amines

Nugent, Thomas C.,Negru, Daniela E.,El-Shazly, Mohamed,Hu, Dan,Sadiq, Abdul,Bibi, Ahtaram,Umar, M. Naveed

, p. 2085 - 2092 (2011/10/19)

Difficult-to-access chiral primary amines were formed in good to high yield and ee using a rare example of a one-pot synthesis from prochiral ketones (sequential reductive amination-hydrogenloysis). As a highlight we also demonstrate a one-pot reductive amination-hydrogenolysis-reductive amination (five reactions) of ortho-methoxyacetophenone resulting in the chiral diamine 1-(2-methoxyphenyl)ethyl-(2-pyridylmethyl)-amine (4) (58% overall yield, >99% ee), a new organocatalyst for aqueous enantioselective aldol reactions. Copyright

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