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2-Fluoro-4-methoxybenzaldehyde is a fluorinated aromatic aldehyde, characterized by its white to off-white crystalline solid appearance. It can be synthesized from 4-bromo-3-fluoroanisole and is known for its unique chemical properties.

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  • 331-64-6 Structure
  • Basic information

    1. Product Name: 2-Fluoro-4-methoxybenzaldehyde
    2. Synonyms: 2-fluor0-4-methoxybenzaldehyde;2-FLUORO-4-METHOXYBENZALDEHYDE;2-FLUORO-P-ANISALDEHYDE;2-Fluoro-4-methoxybenzaldehyde 97%;2-FLUORO-4-METHYLOXYBENZALDEHYDE;2-Fluoro-4-methoxybenzaldehyde97%;2-FLUORO-4-METHYOXYBENZALDEHYDE;2-Fluor-4-methoxybenzaldehyde
    3. CAS NO:331-64-6
    4. Molecular Formula: C8H7FO2
    5. Molecular Weight: 154.14
    6. EINECS: 1806241-263-5
    7. Product Categories: Aromatic Aldehydes & Derivatives (substituted);Benzene series;Benzaldehyde;Adehydes, Acetals & Ketones;Anisoles, Alkyloxy Compounds & Phenylacetates;Fluorine Compounds;Halogenated Heterocycles ,Triazines ,Thiophenes
    8. Mol File: 331-64-6.mol
  • Chemical Properties

    1. Melting Point: 43-48 °C(lit.)
    2. Boiling Point: 226.5 °C at 760 mmHg
    3. Flash Point: >230 °F
    4. Appearance: white to off-white crystalline solid
    5. Density: 1.192 g/cm3
    6. Vapor Pressure: 0.0815mmHg at 25°C
    7. Refractive Index: 1.525
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. Sensitive: Air Sensitive
    11. BRN: 3237954
    12. CAS DataBase Reference: 2-Fluoro-4-methoxybenzaldehyde(CAS DataBase Reference)
    13. NIST Chemistry Reference: 2-Fluoro-4-methoxybenzaldehyde(331-64-6)
    14. EPA Substance Registry System: 2-Fluoro-4-methoxybenzaldehyde(331-64-6)
  • Safety Data

    1. Hazard Codes: Xn,Xi
    2. Statements: 36/37/38-22
    3. Safety Statements: 37/39-26-36
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 331-64-6(Hazardous Substances Data)

331-64-6 Usage

Uses

Used in Pharmaceutical Industry:
2-Fluoro-4-methoxybenzaldehyde is used as a key intermediate in the synthesis of new analogues for phosphodiesterase 10A inhibitors. These inhibitors play a crucial role in the development of treatments for various neurological and psychiatric disorders.
Used in Chemical Synthesis:
2-Fluoro-4-methoxybenzaldehyde serves as a versatile building block in the preparation of various fluorine-containing compounds, such as:
2,4,5-trisubstituted imidazole: These compounds have potential applications in the development of new pharmaceuticals and agrochemicals.
1-(2-fluoro-4-methoxyphenyl)-2-propanone: 2-Fluoro-4-methoxybenzaldehyde can be used in the synthesis of various organic molecules with potential applications in different industries.
6-(2-fluoro-4-methoxyphenyl)fulvene: 2-Fluoro-4-methoxybenzaldehyde may have potential applications in the development of new materials and chemicals.
10-(2-fluoro-4-methoxyphenyl)-6,7,9,10-tetrahydro-1Hfuro[3,4-b]pyrazolo[3,4-f]quinolin-9-one: This complex molecule could be used in the development of novel pharmaceuticals.
Polyhydroquinoline (PHQ): PHQ is a class of compounds with potential applications in the field of materials science and organic chemistry.
3-(2-fluoro-4-methoxyphenyl) acrylic acid methyl ester: 2-Fluoro-4-methoxybenzaldehyde can be used in the synthesis of various polymers and materials with specific properties.

Check Digit Verification of cas no

The CAS Registry Mumber 331-64-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 331-64:
(5*3)+(4*3)+(3*1)+(2*6)+(1*4)=46
46 % 10 = 6
So 331-64-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H7FO2/c1-11-7-3-2-6(5-10)8(9)4-7/h2-5H,1H3

331-64-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (A19726)  2-Fluoro-4-methoxybenzaldehyde, 97%   

  • 331-64-6

  • 1g

  • 292.0CNY

  • Detail
  • Alfa Aesar

  • (A19726)  2-Fluoro-4-methoxybenzaldehyde, 97%   

  • 331-64-6

  • 5g

  • 919.0CNY

  • Detail
  • Alfa Aesar

  • (A19726)  2-Fluoro-4-methoxybenzaldehyde, 97%   

  • 331-64-6

  • 25g

  • 3397.0CNY

  • Detail

331-64-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-4-methoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names fluoro-4-methoxybenzaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:331-64-6 SDS

331-64-6Relevant articles and documents

1-SUBSTITUTED-3- BETA-D-GLUCOPYRANOSYLATED NITROGENOUS HETERO- CYCLIC COMPOUNDS AND MEDICINES CONTAINING THE SAME

-

Page/Page column 23, (2008/06/13)

A compound having an SGLT1 and/or SGLT2 inhibitory activity which is usable as an agent for the prevention or treatment of diabetes, postprandial hyperglycemia, impaired glucose tolerance, diabetic complications, obesity, etc. It is a 1-substituted-3-(β-D

Compositions containing aromatic aldehydes and their use in treatments

-

, (2008/06/13)

Disclosed are pharmaceutical and cosmetic compositions containing aromatic aldehyde compounds. Some of the disclosed compositions are useful as topical therapeutics for treating inflammatory dermatologic conditions. Some of the compositions are useful in transdermal and other systemic dose forms for treating other inflammatory conditions in mammals.

Nitrone derivatives

-

, (2008/06/13)

A compound represented by the figure (1) or a pharmaceutically acceptable salt thereof is useful as medicament for treating retinal degenerative disorders: wherein Ar is optionally substitued phenyl or optionally substituted heteroaryl;. n is 0, 1 or 2; W

Asymmetric synthesis of fluorinated L-tyrosine and meta-L-tyrosines

Monclus, Michel,Masson, Carine,Luxen, Andre

, p. 39 - 44 (2007/10/02)

A convenient asymmetric synthesis of (2S)-2-amino-3-(2-fluoro-5-hydroxyphenyl) propanoic acid, (2S)-2-amino-3-(4-fluoro-3-hydroxyphenyl) propanoic acid and (2S)-2-amino-3-(2-fluoro-4-hydroxyphenyl) propanoic acid is described.Key steps include the synthes

1,3-Diphenylpropane-1,3-diamines, III: Synthesis of 1,3-bis(hydroxy-halogenophenyl)-propane-1,3-diamines and their Pt(II) complexes. Part A: synthesis of the ligands

Kammermeier,Wiegrebe

, p. 547 - 561 (2007/10/02)

The title diamines were prepared according to von Auwer's/Arakawa's procedures starting from appropriately substituted benzaldehydes and actophenones via chalcones, addition of two moles of hydroxylamine, reduction, and separation of diastereomers as N,N'-bisacetamides. - The Pt(II) complexes of the title ligands are described in the following paper.

Ring-Substituted y1,2-Bis(4-hydroxyphenyl)ethylenediamine>dichloroplatinum(II) Complexes: Compounds with a Selective Effect on the Hormone-Dependent Mammary Carcinoma

Karl, Johann,Gust, Ronald,Spruss, Thilo,Schneider, Martin R.,Schoenenberg, Helmut,et al.

, p. 72 - 83 (2007/10/02)

dichloroplatinum(II) complexes with one substituent in the 2-position (CH3, CF3, F, Br, I: meso- and dl-1-PtCl2, meso-(3-5)-PtCl2, meso-(7 and 8)-PtCl2) or two substituents in the 2,6-position (CH3, Cl: meso-2-PtCl2, meso- and dl-6-PtCl2) in both benzene rings were synthesized and tested for estrogenic and toxic activities.Two complexes (meso-6-PtCl2 and meso-7-PtCl2) possess both effects.In comparative tests on estrogen receptor positive and negative mammary tumors in cell culture (MCF 7, ER+ and MDA-MB 231, ER-) and in animals (MXT, ER+ and MXT, ER-, mouse), meso-6-PtCl2 shows a selective effect on the estrogen receptor positive mammary carcinoma.A further increase of efficacy was achieved with the water-soluble (sulfato)platinum(II) derivative (meso-6-PtSO4).On the DMBA-induced hormone dependent mammary carcinoma of the SD rat, meso-6-PtSO4 is significantly more active than its ligand (meso-6) and cisplatin.

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