Search results
Results from the WOW.Com Content Network
Bromobenzaldehyde isomers Common name and systematic name 2-Bromobenzaldehyde [1] 3-Bromobenzaldehyde [2] 4-Bromobenzaldehyde [3] [4] Structure Molecular formula: C 7 H 5 BrO (BrC 6 H 4 COH) Molar mass: 185.020 g/mol Appearance colorless liquid colorless liquid white solid CAS number [6630-33-7] [3132-99-8] [1122-91-4] Properties Density and ...
4-Bromobenzaldehyde, or p-bromobenzaldehyde, is an organobromine compound with the formula BrC 6 H 4 CHO. It is one of three isomers of bromobenzaldehyde . [ 3 ] It displays reactivity characteristic of benzaldehyde and an aryl bromide .
Download QR code; Print/export ... 2-Bromobenzaldehyde; 3-Bromobenzaldehyde; 4-Bromobenzaldehyde ... Text is available under the Creative Commons Attribution ...
The product, CH 3 CH(OCH 2 CH 3) 2, is formally named 1,1-diethoxyethane but is commonly referred to as "acetal". [39] This can cause confusion as "acetal" is more commonly used to describe compounds with the functional groups RCH(OR') 2 or RR'C(OR'') 2 rather than referring to this specific compound — in fact, 1,1-diethoxyethane is also ...
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
3-Bromobenzaldehyde is an isomer of bromobenzaldehyde. It is a colorless viscous liquid. It is a colorless viscous liquid. 3-Bromobenzaldehyde can be prepared from 3-nitrobenzaldehyde .
4-tert-Butylbenzaldehyde is notable as a rare example of industrial-scale electrochemistry. It is produced by BASF and Givaudan (typically as its methanol acetal ) through a double anodic oxidation of 4- tert -butyltoluene on greater than 10,000 ton per year scale.
Aminoacetaldehyde is the organic compound with the formula OHCCH 2 NH 2. Under the usual laboratory conditions, it is unstable, tending instead to undergo self-condensation . [ 1 ] Aminoacetaldehyde diethylacetal is a stable surrogate.