34123-66-5

Basic information

• Product Name: 3-ISOPROPOXY-4-METHOXY-BENZALDEHYDE
• Synonyms: ASINEX-REAG BAS 12524545;ART-CHEM-BB B014199;CHEMBRDG-BB 3014199;3-ISOPROPOXY-4-METHOXY-BENZALDEHYDE;AKOS B014199;TIMTEC-BB SBB009339;3-isopropoxy-4-methoxybenzaldehyde(SALTDATA: FREE);4-methoxy-3-propan-2-yloxybenzaldehyde
• CAS NO: 34123-66-5
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.23
• Mol File: 34123-66-5.mol
• Article Data: 29

Chemical Properties

• Boiling Point: 297.9°C at 760 mmHg
• Flash Point: 124.8°C
• Appearance: /
• Density: 1.064g/cm³
• Vapor Pressure: 0.00131mmHg at 25°C
• Refractive Index: 1.521
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-ISOPROPOXY-4-METHOXY-BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ISOPROPOXY-4-METHOXY-BENZALDEHYDE(34123-66-5)
• EPA Substance Registry System: 3-ISOPROPOXY-4-METHOXY-BENZALDEHYDE(34123-66-5)

Safety Data

• Hazard Codes: Xi
• Statements: 43
• Safety Statements: 36/37
• HazardClass: IRRITANT
• Hazardous Substances Data: 34123-66-5(Hazardous Substances Data)

Usage

Description

3-ISOPROPOXY-4-METHOXY-BENZALDEHYDE is a chemical compound characterized by its molecular formula C11H14O3. It is a pale yellow liquid with a distinctive sweet, floral scent.
Used in Fragrance Industry:
3-ISOPROPOXY-4-METHOXY-BENZALDEHYDE is used as a fragrance ingredient for its sweet, floral odor, enhancing the scent profiles of various consumer products such as perfumes, soaps, and cosmetics.
Used in Pharmaceutical Industry:
3-ISOPROPOXY-4-METHOXY-BENZALDEHYDE is used as a synthetic intermediate in the development and production of pharmaceuticals, contributing to the creation of new medications and organic compounds.
Used in Chemical Synthesis:
3-ISOPROPOXY-4-METHOXY-BENZALDEHYDE is utilized as a key component in the synthesis of other organic compounds, playing a crucial role in advancing chemical research and product development.
Safety Note:
3-ISOPROPOXY-4-METHOXY-BENZALDEHYDE is considered relatively safe for use in consumer products when adhering to industry guidelines and regulations. However, it is essential to handle and store this compound with care and follow proper safety precautions to minimize any potential risks.

InChI:InChI=1/C11H14O3/c1-8(2)14-11-6-9(7-12)4-5-10(11)13-3/h4-8H,1-3H3

Upstream product

• 621-59-0 isovanillin 
• 584-08-7 potassium carbonate 
• 75-26-3 isopropyl bromide 
• 3814-30-0 cyclopentylmethyl bromide 
• 2539-21-1 o-methoxyphenyl i-propyl ether 
• 93-61-8 N-methyl-N-phenylformamide 
• 90-05-1 2-methoxy-phenol 
• 75-30-9 2-iodo-propane 

Downstream Products

• 115439-02-6 3-isopropoxy-4-methoxy-3',4'-methylenedioxychalcone 
• 215715-43-8 β,β-dibromo-3-isopropoxy-4-methoxystyrene 
• 624720-90-7 3-isopropoxy-1-methoxy-4-vinylbenzene 
• 917591-94-7 (3''-isopropoxy-4''-methoxyphenyl)-(5',6',7'-trimethoxy-3',4'-dihydronaphthalen-1'-yl)-methanol 
• 1073537-43-5 (3''-isopropoxy-4''-methoxyphenyl)-(1',2',3'-trimethoxy-8',9'-dihydro-7'H-benzocyclohepten-5'-yl)-methanol 
• 1192217-78-9 3-isopropoxy-4,β-dimethoxystyrene 
• 1213240-88-0 3-isopropoxy-4-methoxy-β-nitrostyrene 
• 1417453-13-4 2’,3,4’-triisopropoxy-4-methoxychalcone 
• 13323-67-6 2’,3,4’-trihydroxy-4-methoxychalcone 
• 621-59-0 isovanillin 
• 1108621-60-8 2-(2-(3-isopropoxy-4-methoxystyryl)-4-isopropoxy-5-methoxyphenyl)ethoxime 
• 1108621-62-0 1-(3-isopropoxy-4-methoxybenzyl)-1,2,3,4-tetrahydro-7-isopropoxy-6-methoxyisoquinoline-N-hydroxide 
• 1108621-35-7 (Z)-2-[-2-(3-isopropoxy-4-methoxystyryl)-4-isopropoxy-5-methoxyphenyl]-N-hydroxyethanamine 
• 1108621-37-9 (Z)-2-[2-(3-isopropoxy-4-methoxystyryl)-4-isopropoxy-5-methoxyphenyl]-N-hydroxy-2-methylprop-2-en-1-amine 

Relevant articles and documents

Lamellarin-inspired potent topoisomerase I inhibitors with the unprecedented benzo[g][1]benzopyrano[4,3-b]indol-6(13H)-one scaffold

A new class of topoisomerase I inhibitors containing the unprecedented benzo[g][1]benzopyrano[4,3-b]indol-6(13H)-one (abbreviated as BBPI) ring system have been developed based on structure-activity relationship studies of the cytotoxic marine alkaloid la

A 2-phenyl-substituted-3-benzoyl-substituted indole preparation method

The invention relates to a preparing method of 2-(phenyl-substituted)-3-(benzoyl-substituted)indole, and particularly discloses a preparing method of 2-(3'-hydroxy-4'-methoxyphenyl)-3-(3'',4'',5''-triethoxybenzoyl)-6-methoxyindole (OXi8006). The structure formula of the OXi8006 is shown in the specification. The OXi8006 can generate good antitumor activity (IC50=1.1 muM) by inhibiting tubulin polymerization and is an important clinical candidate for treating tumor. Synthesis of the OXi8006 by the method has characteristics of simple conditions, easy operation, short reaction steps and high total yield.

Isolation, structure characterization, and synthesis of stabilized 1,2,3,4-tetrahydroisoquinoline marine natural product from potassium cyanide pretreated Thai tunicate, Ecteinascidia thurstoni

A simple 1,2,3,4-tetrahydroisoquinoline marine natural product (2a) together with two known compounds (3 and 4) was isolated from a low polar fraction of the crude extract of KCN pretreated Thai tunicate Ecteinascidia thurstoni. The structure of 2a was de