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CAS

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151726-42-0

3-(benzyloxy)-2-iodo-4-methoxybenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151726-42-0 Structure

  • Basic information

    1. Product Name: 3-(benzyloxy)-2-iodo-4-methoxybenzaldehyde
    2. Synonyms: 3-(benzyloxy)-2-iodo-4-methoxybenzaldehyde
    3. CAS NO:151726-42-0
    4. Molecular Formula:
    5. Molecular Weight: 368.171
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151726-42-0.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: 3-(benzyloxy)-2-iodo-4-methoxybenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(benzyloxy)-2-iodo-4-methoxybenzaldehyde(151726-42-0)
    11. EPA Substance Registry System: 3-(benzyloxy)-2-iodo-4-methoxybenzaldehyde(151726-42-0)

  • 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: 151726-42-0(Hazardous Substances Data)

151726-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151726-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,7,2 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 151726-42:
(8*1)+(7*5)+(6*1)+(5*7)+(4*2)+(3*6)+(2*4)+(1*2)=120
120 % 10 = 0
So 151726-42-0 is a valid CAS Registry Number.

151726-42-0Relevant articles and documents

Enantioselective Synthesis and Racemization of (?)-Sinoracutine

Volpin, Giulio,Vep?ek, Nynke A.,Bellan, Andreas B.,Trauner, Dirk

, p. 897 - 901 (2017)

Sinoracutine is a recently isolated alkaloid with unusual stereochemical and biological properties. It features an unprecedented tetracyclic 6/6/5/5 skeleton that bears an N-methylpyrrolidine ring fused to a cyclopentenone. Interestingly, both enantiomers

Intramolecular Heck cyclization to the galanthamine-type alkaloids: Total synthesis of (±)-lycoramine

Liang, Pi-Hui,Liu, Jing-Ping,Hsin, Ling-Wei,Cheng, Chen-Yu

, p. 11655 - 11660 (2007/10/03)

A novel approach towards the construction of the galanthamine skeleton was demonstrated by the total synthesis of (±)-lycoramine. The key steps include a Pd-catalyzed intramolecular cyclization to form the seven-membered azepane ring and a spontaneous int

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