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461435-05-2

2,4-dihydroxy-3-hydroxymethyl-5-iodo-benzoic 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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  • 461435-05-2 Structure

  • Basic information

    1. Product Name: 2,4-dihydroxy-3-hydroxymethyl-5-iodo-benzoic acid methyl ester
    2. Synonyms: 2,4-dihydroxy-3-hydroxymethyl-5-iodo-benzoic acid methyl ester
    3. CAS NO:461435-05-2
    4. Molecular Formula:
    5. Molecular Weight: 324.072
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 461435-05-2.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: 2,4-dihydroxy-3-hydroxymethyl-5-iodo-benzoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-dihydroxy-3-hydroxymethyl-5-iodo-benzoic acid methyl ester(461435-05-2)
    11. EPA Substance Registry System: 2,4-dihydroxy-3-hydroxymethyl-5-iodo-benzoic acid methyl ester(461435-05-2)

  • 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: 461435-05-2(Hazardous Substances Data)

461435-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 461435-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,1,4,3 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 461435-05:
(8*4)+(7*6)+(6*1)+(5*4)+(4*3)+(3*5)+(2*0)+(1*5)=132
132 % 10 = 2
So 461435-05-2 is a valid CAS Registry Number.

461435-05-2Relevant articles and documents

Total Synthesis of Luminacin D

Shotwell, J. Brad,Krygowski, Evan S.,Hines, John,Koh, Brian,Huntsman, Elliott W. D.,Choi, Hui Won,Schneekloth Jr., John S.,Wood, John L.,Crews, Craig M.

, p. 3087 - 3089 (2002)

(Equation Presented) A highly convergent synthesis of the angiogenesis inhibitor luminacin D has been achieved in 13 linear steps (19 steps total, 5.3% overall yield) utilizing a samarium(II) iodide-mediated mixed tandem aldol/Evans-Tishchenko reaction to

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