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144296-42-4

2-IODOMETHYL-CYCLOPROPANE-1,1-DICARBOXYLIC ACID DIETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1,1-Cyclopropanedicarboxylic acid, 2-(iodomethyl)-, 1,1-diethyl ester

    Cas No: 144296-42-4

  • USD $ 1.9-2.9 / Gram

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  • 144296-42-4 Structure

  • Basic information

    1. Product Name: 2-IODOMETHYL-CYCLOPROPANE-1,1-DICARBOXYLIC ACID DIETHYL ESTER
    2. Synonyms: 2-IODOMETHYL-CYCLOPROPANE-1,1-DICARBOXYLIC ACID DIETHYL ESTER
    3. CAS NO:144296-42-4
    4. Molecular Formula: C10H15IO4
    5. Molecular Weight: 326.12817
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144296-42-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 300.9±12.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.632±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-IODOMETHYL-CYCLOPROPANE-1,1-DICARBOXYLIC ACID DIETHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-IODOMETHYL-CYCLOPROPANE-1,1-DICARBOXYLIC ACID DIETHYL ESTER(144296-42-4)
    11. EPA Substance Registry System: 2-IODOMETHYL-CYCLOPROPANE-1,1-DICARBOXYLIC ACID DIETHYL ESTER(144296-42-4)

  • 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: 144296-42-4(Hazardous Substances Data)

144296-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144296-42-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,9 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144296-42:
(8*1)+(7*4)+(6*4)+(5*2)+(4*9)+(3*6)+(2*4)+(1*2)=134
134 % 10 = 4
So 144296-42-4 is a valid CAS Registry Number.

144296-42-4Relevant articles and documents

Nucleotides and pronucleotides of 2,2-bis(hydroxymethyl) methylenecyclopropane analogues of purine nucleosides: Synthesis and antiviral activity

Yan, Zhaohua,Kern, Earl R.,Gullen, Elizabeth,Cheng, Yung-Chi,Drach, John C.,Zemlicka, Jiri

, p. 91 - 99 (2007/10/03)

Phenylmethylphosphor-L-alaninate pronucleotides 7a, 7b, 8a, and 8b, cyclic phosphates 10a and 10b, and phosphates 11a and 11b derived from 2,2-bis(hydroxymethyl)methylenecyclopropane analogues 1a, 1b, 2a, and 2b were synthesized and evaluated for their an

The iodination and iodocyclisation of some alkenylmalonates

Beckwith, Athelstan L. J.,Tozer, Matthew J.

, p. 4975 - 4978 (2007/10/02)

Consecutive treatment of various allylmalonates with sodium hydride and iodine in THF affords cyclopropane derivatives via intermediate formation of iodomalonates; iodocyclisation under similar conditions affords cyclopentane and cyclohexane derivatives from appropriate alkenylmalonates.

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