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19434-36-7

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19434-36-7 Usage

General Description

2-(4-Methoxyphenoxy)benzenecarbaldehyde is a chemical compound with the molecular formula C15H14O3. It is a white to light yellow crystalline powder and is used primarily as a building block in the synthesis of pharmaceuticals and agrochemicals. 2-(4-METHOXYPHENOXY)BENZENECARBALDEHYDE has a wide range of potential applications, including as an intermediate in the production of dyes, pigments, and other organic compounds. It is also used in the synthesis of materials such as polymers and resins. Additionally, 2-(4-Methoxyphenoxy)benzenecarbaldehyde is also used as a fragrance ingredient in perfumes and personal care products. While it has several industrial and commercial applications, this compound should be handled and processed with care due to its potential health and safety hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 19434-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,3 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19434-36:
(7*1)+(6*9)+(5*4)+(4*3)+(3*4)+(2*3)+(1*6)=117
117 % 10 = 7
So 19434-36-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H12O3/c1-16-12-6-8-13(9-7-12)17-14-5-3-2-4-11(14)10-15/h2-10H,1H3

19434-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenoxy)benzaldehyde

1.2 Other means of identification

Product number -
Other names methoxyphenoxybenzenecarbaldehyde

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:19434-36-7 SDS

19434-36-7Relevant articles and documents

Mildness in preparative conditions directly affects the otherwise straightforward syntheses outcome of Schiff-base isoniazid derivatives: Aroylhydrazones and their solvolysis-related dihydrazones

Cukierman, Daphne S.,Evangelista, Beatriz N.,Neto, Carlos Castanho,Franco, Chris H.J.,Costa, Luiz Ant?nio S.,Diniz, Renata,Limberger, Jones,Rey, Nicolás A.

, (2020/10/20)

Aroylhydrazones are versatile compounds with a series of applications, from biological to technological spheres. The simplicity of their preparation allows for a great chemical variability and synthetic manageability. However, the process can be not as st

Formation and Disproportionation of Xanthenols to Xanthenes and Xanthones and Their Use in Synthesis

Shi, Zeyu,Chen, Si,Xiao, Qiong,Yin, Dali

, p. 3334 - 3343 (2021/02/05)

A facile and versatile strategy employing TiCl4-mediated cyclization followed by a Cannizzaro reaction has been developed for the synthesis of various xanthene derivatives. The reaction proceeded smoothly to afford both xanthenes/xanthones or their sulfur derivatives and tolerated a wide range of electronically diverse substrates. Using this methodology, pranoprofen was synthesized in three steps in 59% overall yield from commercially available starting materials.

Pyrimidine onium compound and application thereof

-

Paragraph 0431-0434, (2019/10/23)

The invention relates to a pyrimidine onium compound, nitride oxides, salt of the nitride oxides and a composition comprising the compound. The invention further relates to an application of the compound to plant pest control.

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