2215-76-1 Usage
Description
4-(4-Formylphenoxy)benzaldehyde 96, a benzaldehyde derivative with the chemical formula C14H10O3, is a yellow crystalline solid. It features a formyl group attached to a phenoxy group on the 4-position of the benzene ring, contributing to its molecular weight of 226.22 g/mol. 4-(4-FORMYLPHENOXY)BENZALDEHYDE 96 is utilized in organic synthesis and serves as a building block for the creation of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it functions as a reagent for preparing other organic compounds. Due to its potential irritant and flammable properties, 4-(4-Formylphenoxy)benzaldehyde 96 is typically handled and stored under controlled laboratory conditions.
Uses
Used in Pharmaceutical Industry:
4-(4-Formylphenoxy)benzaldehyde 96 is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(4-Formylphenoxy)benzaldehyde 96 is employed as a precursor for the production of agrochemicals. Its incorporation into these compounds can enhance their effectiveness in pest control and crop protection, thereby supporting agricultural productivity.
Used in Organic Synthesis:
4-(4-Formylphenoxy)benzaldehyde 96 is used as a building block in organic synthesis for the creation of a wide range of fine chemicals. Its versatility in chemical reactions enables the production of specialty chemicals used in various industries, including fragrances, dyes, and coatings.
Used as a Reagent:
4-(4-FORMYLPHENOXY)BENZALDEHYDE 96 also serves as a reagent in the preparation of other organic compounds. Its reactivity and functional groups make it a valuable tool in the synthesis of complex organic molecules, facilitating research and development in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 2215-76-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2215-76:
(6*2)+(5*2)+(4*1)+(3*5)+(2*7)+(1*6)=61
61 % 10 = 1
So 2215-76-1 is a valid CAS Registry Number.
2215-76-1Relevant articles and documents
Bis-Benzyl-Tetrahydroisoquinoline Derivatives As Therapeutics For Filovirus
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Paragraph 0058; 0059, (2019/09/20)
Bis-benzyl-tetrahydroisoquinoline analogs that are derivatives of the cyclic products tetrandrine (TETN) and cepharanthine (CEPH). The analogs indicate activity against filovirus infections, including the type species Marburg virus (MARV) and Ebola virus (EBOV).
Styrene-based compound and preparation method and application thereof
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Paragraph 0077; 0079; 0081; 0082; 0083; 0084; 0085-0094, (2018/07/15)
The invention discloses a styrene-based compound, which is at least a 5-(4-(4-(3,5-dyhydroxystyryl)phenoxyl)styryl)-1,3-benzenediol compound of the following structural formula. The invention also discloses a preparation method and application of the 5-(4-(4-(3,5-dyhydroxystyryl)phenoxyl)styryl)-1,3-benzenediol compound of the structural formula. The 5-(4-(4-(3,5-dyhydroxystyryl)phenoxyl)styryl)-1,3-benzenediol compound disclosed by the invention is used for inhibiting the abnormal growth of B-cells by lowering AKT/mTOR signal conduction. The formula is shown in the specification.
Highly efficient heterogeneous copper-catalysed O-arylation of phenols by nitroarenes leading to diaryl ethers
Du, Yingying,Yao, Fang,Tuo, Yuxin,Cai, Mingzhong
, p. 725 - 729 (2018/01/08)
The heterogeneous O-arylation of phenols by nitroarenes was achieved in DMF at 100 °C by using an MCM-41-immobilised bidentate nitrogen copper(II) complex [MCM-41-2N-Cu(OAc)2] as catalyst, yielding a variety of unsymmetrical diaryl ethers in good to excellent yields. This heterogeneous copper catalyst can be easily prepared by a simple procedure from commercially readily available and inexpensive reagents, recovered by filtration of the reaction solution and recycled at least seven times without significant loss of activity.