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2,2-dimethyl-2-(2-iodoxyphenyl)acetic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1240324-79-1 Structure
  • Basic information

    1. Product Name: 2,2-dimethyl-2-(2-iodoxyphenyl)acetic acid methyl ester
    2. Synonyms: 2,2-dimethyl-2-(2-iodoxyphenyl)acetic acid methyl ester
    3. CAS NO:1240324-79-1
    4. Molecular Formula:
    5. Molecular Weight: 336.126
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1240324-79-1.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: 2,2-dimethyl-2-(2-iodoxyphenyl)acetic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-dimethyl-2-(2-iodoxyphenyl)acetic acid methyl ester(1240324-79-1)
    11. EPA Substance Registry System: 2,2-dimethyl-2-(2-iodoxyphenyl)acetic acid methyl ester(1240324-79-1)
  • 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: 1240324-79-1(Hazardous Substances Data)

1240324-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1240324-79-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,0,3,2 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1240324-79:
(9*1)+(8*2)+(7*4)+(6*0)+(5*3)+(4*2)+(3*4)+(2*7)+(1*9)=111
111 % 10 = 1
So 1240324-79-1 is a valid CAS Registry Number.

1240324-79-1Downstream Products

1240324-79-1Relevant articles and documents

New chiral hypervalent iodine(V) compounds as stoichiometric oxidants

Altermann, Sabine M.,Sch?fer, Sascha,Wirth, Thomas

experimental part, p. 5902 - 5907 (2010/09/08)

The synthesis and application of some new hypervalent iodine compounds bearing chiral and achiral ester motives derived from easily accessible starting materials is presented. The oxidation is carried out using dimethyldioxirane as an oxidant providing the desired compounds in moderate to high yields. A crystal structure analysis for one iodine(V) derivative is investigated. The λ5-iodanes are applied as stoichiometric reagents in the oxidation of thioanisole to phenylmethyl sulfoxide, benzyl alcohol to benzaldehyde, and meso-hydrobenzoine to benzaldehyde, benzyl, and benzoin.

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