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  2. Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Bromobenzaldehyde

    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 ...

  3. 4-Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-bromobenzaldehyde

    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.

  4. 3-Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/3-Bromobenzaldehyde

    Chemical formula. C 7 H 5 Br O: Molar mass: 185.020 g·mol −1 Appearance ... 3-Bromobenzaldehyde is an isomer of bromobenzaldehyde. It is a colorless viscous liquid.

  5. C7H5BrO - Wikipedia

    en.wikipedia.org/wiki/C7H5BrO

    The molecular formula C 7 H 5 BrO may refer to: ... 3-Bromobenzaldehyde; 4-Bromobenzaldehyde; Bromotropone This page was last edited on 24 October 2023, at 23 ...

  6. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    Its chemical formula is C 6 H 5 Br. It is a colourless liquid although older samples can appear yellow. It is a colourless liquid although older samples can appear yellow. It is a reagent in organic synthesis .

  7. Benzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde

    Amygdalin 2 H 2 O HCN benzaldehyde 2 × glucose 2 × Benzaldehyde contributes to the scent of oyster mushrooms (Pleurotus ostreatus). Reactions Benzaldehyde is easily oxidized to benzoic acid in air at room temperature, causing a common impurity in laboratory samples. Since the boiling point of benzoic acid is much higher than that of benzaldehyde, it may be purified by distillation. Benzyl ...

  8. NanoPutian - Wikipedia

    en.wikipedia.org/wiki/Nanoputian

    One of the bromine substituents is converted to an aldehyde through an S N 2 reaction with the strong base, n-BuLi, and THF in the aprotic polar solvent, DMF to produce 2,5-bis(4-tert-butyldimethylsiloxy-1′-butynyl)-4-bromobenzaldehyde. Another Sonogashira coupling with 3,5-(1′-Pentynyl)-1-ethynylbenzene attaches the lower body of the ...

  9. Benzyl bromide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_bromide

    Benzyl bromide is an organic compound with the formula C 6 H 5 CH 2 Br. The molecule consists of a benzene ring substituted with a bromomethyl group. It is a colorless liquid with lachrymatory properties. The compound is a reagent for introducing benzyl groups. [3] [4]