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1037831-19-8

4-fluoro-1-iodo-2-methoxymethoxy-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1037831-19-8 Structure

  • Basic information

    1. Product Name: 4-fluoro-1-iodo-2-methoxymethoxy-benzene
    2. Synonyms: 4-fluoro-1-iodo-2-methoxymethoxy-benzene
    3. CAS NO:1037831-19-8
    4. Molecular Formula:
    5. Molecular Weight: 282.053
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1037831-19-8.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: 4-fluoro-1-iodo-2-methoxymethoxy-benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-fluoro-1-iodo-2-methoxymethoxy-benzene(1037831-19-8)
    11. EPA Substance Registry System: 4-fluoro-1-iodo-2-methoxymethoxy-benzene(1037831-19-8)

  • 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: 1037831-19-8(Hazardous Substances Data)

1037831-19-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1037831-19-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,8,3 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1037831-19:
(9*1)+(8*0)+(7*3)+(6*7)+(5*8)+(4*3)+(3*1)+(2*1)+(1*9)=138
138 % 10 = 8
So 1037831-19-8 is a valid CAS Registry Number.

1037831-19-8Relevant articles and documents

An intra/intermolecular suzuki sequence to benzopyridyloxepines containing geometrically pure exocyclic tetrasubstituted alkenes

Carson, Matthew W.,Giese, Matthew W.,Coghlan, Michael J.

supporting information; experimental part, p. 2701 - 2704 (2009/05/26)

(Chemical Equation Presented) A route to enable the preparation of 5-benzylidenyl-benzopyridyloxepine analogues was developed to continue our research in the field of nuclear hormone receptor modulators. The key steps are1) a syn-stereoselective diboratio

Synthesis of constrained arylpiperidines using intramolecular Heck or radical reactions

Morice, Christophe,Domostoj, Mathias,Briner, Karin,Mann, André,Suffert, Jean,Wermuth, Camille-Georges

, p. 6499 - 6502 (2007/10/03)

Two intramolecular routes were experimented to reach the hexahydrobenzofuro[2,3-c]pyridine platform: a Heck and a radical reaction. The radical route was applicable to all substrates, whereas the Heck route was of limited use. The key adducts were obtained via a Mitsunobu condensation between halogenated phenols and an allylic alcohol, the 3-hydroxy-tetrahydropyridine.

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