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126940-12-3

2-fluoro-6-methoxymethoxybenzaldehyde oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126940-12-3 Structure

  • Basic information

    1. Product Name: 2-fluoro-6-methoxymethoxybenzaldehyde oxime
    2. Synonyms: 2-fluoro-6-methoxymethoxybenzaldehyde oxime
    3. CAS NO:126940-12-3
    4. Molecular Formula:
    5. Molecular Weight: 199.182
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126940-12-3.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-fluoro-6-methoxymethoxybenzaldehyde oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-fluoro-6-methoxymethoxybenzaldehyde oxime(126940-12-3)
    11. EPA Substance Registry System: 2-fluoro-6-methoxymethoxybenzaldehyde oxime(126940-12-3)

  • 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: 126940-12-3(Hazardous Substances Data)

126940-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126940-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,9,4 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126940-12:
(8*1)+(7*2)+(6*6)+(5*9)+(4*4)+(3*0)+(2*1)+(1*2)=123
123 % 10 = 3
So 126940-12-3 is a valid CAS Registry Number.

126940-12-3Relevant articles and documents

A Novel Synthesis of 3-Amino-1,2-benzisoxazoles - an Entry into the Isoxazolobenzoxazepine Ring System

Shutske, Gregory M.,Kapples, Kevin J.

, p. 1293 - 1298 (2007/10/02)

A novel synthesis of 3-amino-1,2-benzisoxazole (3) from 2-benzonitrile (2) is described.This methodology was used to synthesize 3-amino-4-hydroxy-1,2-benzisoxazole (10), which served as an intermediate for a number of isoxazolo3

Necic Acid Synthons. Part 2. Regioselectivity in the Reactions of (Z)-2-Bromomethyl-2-alkenoate Esters with Selected Carbon Nucleophiles

Ameer, Farouk,Drewes, Siegfried E.,Emslie, Neville D.,Kaye, Perry T.,Mann, R. Leigh

, p. 2293 - 2295 (2007/10/02)

The preparation of selected (Z)-2-bromomethyl-2-alkenoate esters and their subsequent reaction with acetoacetic ester-derived nucleophiles is described.Both the substrate structure and the solvent system have significant effects on the regioselectivity of these nucleophilic displacements.

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