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1,1-dimethylethyl 4-fluoro-3-hydroxy-3-methyl-2-(phenylmethoxy)butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 119620-25-6 Structure
  • Basic information

    1. Product Name: 1,1-dimethylethyl 4-fluoro-3-hydroxy-3-methyl-2-(phenylmethoxy)butanoate
    2. Synonyms:
    3. CAS NO:119620-25-6
    4. Molecular Formula:
    5. Molecular Weight: 298.355
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 119620-25-6.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: 1,1-dimethylethyl 4-fluoro-3-hydroxy-3-methyl-2-(phenylmethoxy)butanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1-dimethylethyl 4-fluoro-3-hydroxy-3-methyl-2-(phenylmethoxy)butanoate(119620-25-6)
    11. EPA Substance Registry System: 1,1-dimethylethyl 4-fluoro-3-hydroxy-3-methyl-2-(phenylmethoxy)butanoate(119620-25-6)
  • 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: 119620-25-6(Hazardous Substances Data)

119620-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119620-25-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,6,2 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119620-25:
(8*1)+(7*1)+(6*9)+(5*6)+(4*2)+(3*0)+(2*2)+(1*5)=116
116 % 10 = 6
So 119620-25-6 is a valid CAS Registry Number.

119620-25-6Downstream Products

119620-25-6Relevant articles and documents

Purification and Inhibition of Spinach &α,&β-Dihydroxyacid Dehydratase

Pirrung, Michael C.,Ha, Hyun-Joon,Holmes, Christopher P.

, p. 1543 - 1548 (1989)

The α,β-dihydroxyacid dehydratase (E.C. 4.2.1.9) responsible for the production of α-oxoisovaleric acid in the valine biosynthetic pathway has been purified from spinach leaves.Its properities are similar to those given in a previous report using a less pure preparation.Its monomer mass is estimated to be 55 kDa.Evidence for an enol intermediate in the reaction mechanism has been obtained by a deuterium labeling study.Several inhibitors have been screened against the enzyme.Four of particular effectiveness are 4-fluoro-3,3-dihydroxyisovaleric acid, 1-hydroxy-1-isobutanesulfonic acid, N,N-dimethylglycine N-oxide, and 2-fluoro-3,3-dimethylacrylic acid.As an enol analogue, the latter compound gives further evidence for enol itermediate.

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