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1304127-09-0

(R)-1-fluoro-4-[(4-methoxyphenyl)amino]heptan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1304127-09-0 Structure

  • Basic information

    1. Product Name: (R)-1-fluoro-4-[(4-methoxyphenyl)amino]heptan-2-one
    2. Synonyms: (R)-1-fluoro-4-[(4-methoxyphenyl)amino]heptan-2-one
    3. CAS NO:1304127-09-0
    4. Molecular Formula:
    5. Molecular Weight: 253.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1304127-09-0.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: (R)-1-fluoro-4-[(4-methoxyphenyl)amino]heptan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-1-fluoro-4-[(4-methoxyphenyl)amino]heptan-2-one(1304127-09-0)
    11. EPA Substance Registry System: (R)-1-fluoro-4-[(4-methoxyphenyl)amino]heptan-2-one(1304127-09-0)

  • 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: 1304127-09-0(Hazardous Substances Data)

1304127-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1304127-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,4,1,2 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1304127-09:
(9*1)+(8*3)+(7*0)+(6*4)+(5*1)+(4*2)+(3*7)+(2*0)+(1*9)=100
100 % 10 = 0
So 1304127-09-0 is a valid CAS Registry Number.

1304127-09-0Downstream Products

1304127-09-0Relevant articles and documents

Highly enantioselective synthesis of fluorinated β-amino ketones via asymmetric organocatalytic Mannich reactions: A case study of unusual reversal of regioselectivity

Lu, Min,Lu, Yunpeng,Tan, Puay Kah Amy,Lau, Qiu Ying,Zhong, Guofu

, p. 477 - 480 (2011)

The highly enantioselective direct Mannich protocol employing fluoroacetone, p-anisidine, and aldehydes catalyzed by 4-siloxyproline was developed, allowing efficient access for pharmaceutically important fluorinated β-amino ketones. On the basis of DFT c

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