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  2. 4-Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-bromobenzaldehyde

    CAS Number. ... 4-Bromobenzaldehyde, or p-bromobenzaldehyde, is an organobromine compound with the formula BrC 6 H 4 CHO. It is one of three isomers of ...

  3. 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 ...

  4. 4-Formylphenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/4-Formylphenylboronic_acid

    The synthesis of 4-formylyphenylboronic acid was reported by the group of Heinrich Nöth in 1990. 4-Bromobenzaldehyde was used as starting material. [2] The acetalization of the aldehyde group was carried out by standard methods [3] using diethoxymethoxyethane and ethanol to give 1-bromo-4-(diethoxymethyl)benzene.

  5. 3-Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/3-Bromobenzaldehyde

    CAS Number. 3132-99-8; 3D model ... 3-Bromobenzaldehyde is an isomer of ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; ...

  6. 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 ...

  7. 4-Ethynylbenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-ethynylbenzaldehyde

    4-Ethynylbenzaldehyde may be prepared by the Sonogashira coupling of 4-bromobenzaldehyde with trimethylsilylacetylene to form 4-((trimethylsilyl)ethynyl)benzaldehyde, followed by removal of the trimethylsilyl group with base to form 4-ethynylbenzaldehyde. [3]

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  9. 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 ...