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methyl 2-butyl-3-fluorobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1254176-30-1 Structure
  • Basic information

    1. Product Name: methyl 2-butyl-3-fluorobenzoate
    2. Synonyms: methyl 2-butyl-3-fluorobenzoate
    3. CAS NO:1254176-30-1
    4. Molecular Formula:
    5. Molecular Weight: 210.248
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1254176-30-1.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: methyl 2-butyl-3-fluorobenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-butyl-3-fluorobenzoate(1254176-30-1)
    11. EPA Substance Registry System: methyl 2-butyl-3-fluorobenzoate(1254176-30-1)
  • 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: 1254176-30-1(Hazardous Substances Data)

1254176-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1254176-30-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,1,7 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1254176-30:
(9*1)+(8*2)+(7*5)+(6*4)+(5*1)+(4*7)+(3*6)+(2*3)+(1*0)=141
141 % 10 = 1
So 1254176-30-1 is a valid CAS Registry Number.

1254176-30-1Downstream Products

1254176-30-1Relevant articles and documents

Efficient preparation of polyfunctional organometallics via directed ortho -metalation

Wunderlich, Stefan H.,Bresser, Tomke,Dunst, Cora,Monzon, Gabriel,Knochel, Paul

, p. 2670 - 2678 (2010)

Highly functionalized organometallics are efficiently prepared in larger quantities (up to 4 g) by directed ortho-metalation using the previously reported amide bases TMP2Mn2MgCl24LiCl (TMP=2,2,6,6-tetramethylpiperidyl), TMP2Fe2MgCl24LiCl and TMP3La3MgCl25LiCl. The resulting organometallics undergo various reactions with electrophiles like acid chlorides, alkyl iodides, or aldehydes and provide the corresponding products in good to excellent yields. Georg Thieme Verlag Stuttgart New York.

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