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58662-54-7

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58662-54-7 Usage

Description

5-(Benzyloxy)-2-Nitrobenzaldehyde is an organic compound that serves as a crucial intermediate in the synthesis of various chemical compounds. It is characterized by its molecular structure, which includes a benzyloxy group attached to the 5th position and a nitro group at the 2nd position of a benzene ring, with an aldehyde group attached to the 1st position.

Uses

Used in Pharmaceutical Industry:
5-(Benzyloxy)-2-Nitrobenzaldehyde is used as an intermediate in the synthesis of 5-Hydroxyindole-3-Acetic Acid-13C3 (H953604), which is an isotope-labeled analog of 5-hydroxyindole-3-acetic acid. 5-(BENZYLOXY)-2-NITROBENZALDEHYDE is an impurity found in chlorpheniramine (C424300), an antihistaminic agent. The use of 5-(Benzyloxy)-2-Nitrobenzaldehyde in this context is essential for the development and production of pharmaceuticals that target histamine-related conditions, such as allergies and other immune responses.

Check Digit Verification of cas no

The CAS Registry Mumber 58662-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,6 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58662-54:
(7*5)+(6*8)+(5*6)+(4*6)+(3*2)+(2*5)+(1*4)=157
157 % 10 = 7
So 58662-54-7 is a valid CAS Registry Number.

58662-54-7Relevant articles and documents

ESTROGEN RECEPTOR-MODULATING COMPOUNDS

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Paragraph 000245; 000295, (2019/08/08)

Described herein are compounds that are estrogen receptor modulators of formula I' Also described are pharmaceutical compositions and medicaments that include the compounds described herein, as well as methods of using such estrogen receptor modulators, alone and in combination with other compounds, for treating diseases or conditions that are mediated or dependent upon estrogen receptors.

Step-economical synthesis of tetrahydroquinolines by asymmetric relay catalytic Friedlaender condensation/transfer hydrogenation

Ren, Lei,Lei, Tao,Ye, Jia-Xi,Gong, Liu-Zhu

supporting information; experimental part, p. 771 - 774 (2012/02/05)

Two steps in one reaction: The title relay reaction relies on a combination of an achiral Lewis acid and a chiral Bronsted acid (B-H in the scheme). This one-pot method provides access to tetrahydroquinoline derivatives with multiple continuous stereogeni

Bronsted acid-catalyzed enantioselective Friedlaender condensations: Achiral amine promoter plays crucial role in the stereocontrol

Ren, Lei,Lei, Tao,Gong, Liu-Zhu

supporting information; experimental part, p. 11683 - 11685 (2011/12/02)

A highly enantioselective Friedlaender condensation has been established by using chiral Bronsted acids in combination with achiral amines to give quinolines in high yields (up to 99%) and with excellent enantioselectivities (up to 95%).

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