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1046338-37-7

C18H19INO2(1+)*I(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1046338-37-7 Structure

  • Basic information

    1. Product Name: C18H19INO2(1+)*I(1-)
    2. Synonyms: C18H19INO2(1+)*I(1-)
    3. CAS NO:1046338-37-7
    4. Molecular Formula:
    5. Molecular Weight: 535.163
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1046338-37-7.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: C18H19INO2(1+)*I(1-)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H19INO2(1+)*I(1-)(1046338-37-7)
    11. EPA Substance Registry System: C18H19INO2(1+)*I(1-)(1046338-37-7)

  • 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: 1046338-37-7(Hazardous Substances Data)

1046338-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1046338-37-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,3,3 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1046338-37:
(9*1)+(8*0)+(7*4)+(6*6)+(5*3)+(4*3)+(3*8)+(2*3)+(1*7)=137
137 % 10 = 7
So 1046338-37-7 is a valid CAS Registry Number.

1046338-37-7Upstream product

1046338-37-7Downstream Products

1046338-37-7Relevant articles and documents

Efficient synthesis of highly substituted indolizinones via iodocyclization and 1,2-shift

Choi, Jihyun,Ge, Hyeong Lee,Kim, Ikyon

, p. 1243 - 1249 (2008)

The 5-endo-dig iodocyclization of propargylic alcohols followed by a 1,2-shift provided rapid access to 2-iodoindolizinones, while the 5-endo-trig iodocyclization of allylic alcohols and subsequent dehydroiodination and 1,2-shift led to indolizinones. A number of highly substituted indolizinones were constructed under these mild reaction conditions. Georg Thieme Verlag Stuttgart.

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