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  2. 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 .

  3. Methyl benzoate - Wikipedia

    en.wikipedia.org/wiki/Methyl_benzoate

    Methyl benzoate is an organic compound. It is an ester with the chemical formula C 6 H 5 COOCH 3, sometimes abbreviated as PhCO 2 Me, where Ph and Me are phenyl and methyl, respectively. Its structure is C 6 H 5 −C(=O)−O−CH 3. It is a colorless liquid that is poorly soluble in water, but miscible with organic solvents.

  4. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    184.5 °c (364.1 °f; 457.7 k) Benzyl bromide is an isomer, which has a bromine substituted for one of the hydrogens of toluene 's methyl group, and it is sometimes named α-bromotoluene. Preparation

  5. 4-Bromophenylacetic acid - Wikipedia

    en.wikipedia.org/wiki/4-Bromophenylacetic_acid

    4-Bromophenylacetic acid may be prepared by the addition of a bromine atom to phenylacetic acid through electrophilic aromatic substitution.It was first prepared in the laboratory by treatment of phenylacetic acid with bromine and mercuric oxide; a mixture of the 2- and 4- isomers is made, and the 4- isomer is isolated by fractional crystallization.

  6. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    [4] Phase transition from orthorhombic Pmn21 phase III at low temperatures (measurements from 95 K), to a disordered rhombohedral phase II at 205-213 K. Phase II can exist from 213-223 K, partly coincident with an FCC phase I, which can be observed between 210-250 K. Phase transitions have also been studied at high pressure (up to 300MPa) [ 5 ]

  7. Diazo - Wikipedia

    en.wikipedia.org/wiki/Diazo

    Examples are the synthesis of tert-butyl diazoacetate [8] and diazomalonate. [9] Methyl phenyldiazoacetate is generated in this way by treating methyl phenylacetate with p-acetamidobenzenesulfonyl azide in the presence of base. [10] [11] Solid state structure of the diazo compound t-BuO 2 CC(N 2)C 6 H 4 NO 2. Key distances: C-N = 1.329 Å, N-N ...

  8. 3-Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/3-Nitrobenzoic_acid

    3-Nitrobenzoic acid is an organic compound with the formula C 6 H 4 (NO 2)CO 2 H. It is an aromatic compound and under standard conditions, it is an off-white solid. The two substituents are in a meta position with respect to each other, giving the alternative name of m-nitrobenzoic acid.

  9. Methyl 2-bromoacetate - Wikipedia

    en.wikipedia.org/wiki/Methyl_2-bromoacetate

    Methyl bromoacetate is an alkylating agent. It has been used to alkylate phenol and amino groups. [4] [5] Moreover, it can be used to make vitamins and pharmaceutical drugs. It is commonly used as a reagent in chemical modification of histidine. [2] In addition, methyl bromoacetate also use in synthesize of coumarins and cis-cyclopropane.