4-N-PROPOXYBENZALDEHYDE

4-N-PROPOXYBENZALDEHYDE

Product Introduction

4-N-PROPOXYBENZALDEHYDE Basic information
Product Name: 4-N-PROPOXYBENZALDEHYDE
Synonyms: TIMTEC-BB SBB008225;P-PROPOXYBENZALDEHYDE;OTAVA-BB BB7020401736;4-propoxy-benzaldehyd;Benzaldehyde, 4-propoxy-;NSC 406729;NSC 32509;Benzaldehyde, p-propoxy-
CAS: 5736-85-6
MF: C10H12O2
MW: 164.2
EINECS:  
Product Categories: Benzaldehyde (Building Blocks for Liquid Crystals);Building Blocks for Liquid Crystals;Functional Materials;Aldehydes;C10 to C21;Carbonyl Compounds;Building Blocks;C10-C12;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
Mol File: 5736-85-6.mol
4-N-PROPOXYBENZALDEHYDE Structure
 
4-N-PROPOXYBENZALDEHYDE Chemical Properties
Melting point 268 °C
Boiling point 129-130 °C/10 mmHg (lit.)
density 1.039 g/mL at 25 °C (lit.)
refractive index n20/D 1.546(lit.)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form clear liquid
Specific Gravity 1.06
color Colorless to Light orange to Yellow
Sensitive Air Sensitive
BRN 743408
CAS DataBase Reference 5736-85-6(CAS DataBase Reference)
EPA Substance Registry System Benzaldehyde, 4-propoxy- (5736-85-6)
 
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38
Safety Statements 26-27-36/37/39
WGK Germany 3
RTECS CU7700000
TSCA T
HazardClass IRRITANT
HS Code 29124990
 
MSDS Information
Provider Language
SigmaAldrich English
ALFA English
 
4-N-PROPOXYBENZALDEHYDE Usage And Synthesis
Chemical Properties White liquid
Uses 4-Propoxybenzaldehyde was used in the preparation of (2S,4S,5R)-(±)-2-(4-propoxyphenyl)-3,4-dimethyl-5-phenyl-1,3-oxazolidine via condensation with 1-ephedrine.
General Description Kinetic constants for the inhibition of the diphenolase activity of mushroom tyrosinase by 4-propoxybenzaldehyde was evaluated.
 
4-N-PROPOXYBENZALDEHYDE Preparation Products And Raw materials
Raw materials Ethyl acetate-->Sodium-->PETROLEUM ETHER-->1-Butanol-->4-Fluorobenzaldehyde
Preparation Products 3-(4-PROPOXYPHENYL)PROPIONIC ACID-->4-Propoxylmandelic acid-->(4-propoxyphenyl)methanol-->3-(4-PROPOXYPHENYL)ACRYLIC ACID

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