212621-51-7

Basic information

• Product Name: 3-METHOXY-4-(1-NAPHTHYLMETHOXY)BENZALDEHYDE
• Synonyms: 3-METHOXY-4-(1-NAPHTHYLMETHOXY)BENZALDEHYDE;3-METHOXY-4-(NAPHTHALEN-1-YLMETHOXY)-BENZALDEHYDE;ASISCHEM T17305
• CAS NO: 212621-51-7
• Molecular Formula: C₁₉H₁₆O₃
• Molecular Weight: 292.33
• Mol File: 212621-51-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 482.5±30.0 °C(Predicted)
• Appearance: /
• Density: 1.198±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 3-METHOXY-4-(1-NAPHTHYLMETHOXY)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-METHOXY-4-(1-NAPHTHYLMETHOXY)BENZALDEHYDE(212621-51-7)
• EPA Substance Registry System: 3-METHOXY-4-(1-NAPHTHYLMETHOXY)BENZALDEHYDE(212621-51-7)

Safety Data

• Hazardous Substances Data: 212621-51-7(Hazardous Substances Data)

Usage

Chemical class

Benzaldehyde derivative

Functional groups

Methoxy group and naphthylmethoxy group

Use

Used in organic synthesis as a building block for pharmaceuticals, agrochemicals, and dyes

Biological activities

Antifungal and antimicrobial properties

Unique reactivity

Presence of both methoxy and naphthylmethoxy groups

Upstream product

• 121-33-5 vanillin 
• 86-52-2 1-Chloromethylnaphthalene 

Downstream Products

• 1264751-10-1 (5Z)-4-amino-5-{[3-methoxy-4-(naphthalen-1-ylmethoxy)phenyl]methylidene}-1,3-thiazol-2(5H)-one 
• 1264751-13-4 (5Z)-5-{[3-methoxy-4-(naphthalen-1-ylmethoxy)phenyl]methylidene}-4-(methylamino)-1,3-thiazol-2(5H)-one 
• 1264753-59-4 (5Z)-5-{[3-methoxy-4-(naphthalen-1-ylmethoxy)phenyl]methylidene}-4-thioxo-1,3-thiazolidin-2-one 
• 1264753-57-2 (5Z)-5-{[3-methoxy-4-(naphthalen-1-ylmethoxy)phenyl]methylidene}-1,3-thiazolidine-2,4-dione 

Relevant articles and documents

Facile synthesis of novel dithioacetal-naphthalene derivatives as potential activators for plant resistance induction

In this paper, a series of novel dithioacetal-naphthalenes were designed and synthesized for plant immunity. Their antiviral activities were evaluated against tobacco mosaic virus (TMV) and cucumber mosaic virus (CMV). The results indicated that most compounds exhibited better activity against CMV than against TMV. These dithioacetal derivatives also displayed good bacterial activity against rice bacterial leaf blight. Among them, compound S16 exhibited relatively good anti-CMV, anti-TMV, and antibacterial activity. Structure-activity relationships indicated that introducing the naphthalene moiety enhanced their activities for plant resistance induction. Therefore, the basic motif of compound S16 could be the most promising candidate for further structural optimization to develop a potential activator for plant resistance induction.

PROPHYLACTIC OR THERAPEUTIC AGENT FOR CANCER

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