4-Bromobenzyl bromide
4-Bromobenzyl bromide structure
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Common Name | 4-Bromobenzyl bromide | ||
|---|---|---|---|---|
| CAS Number | 3433-80-5 | Molecular Weight | 249.930 | |
| Density | 1.9±0.1 g/cm3 | Boiling Point | 253.0±15.0 °C at 760 mmHg | |
| Molecular Formula | C7H6Br2 | Melting Point | 29-32 °C(lit.) | |
| MSDS | USA | Flash Point | 118.0±19.6 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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Distributed Drug Discovery, Part 3: using D(3) methodology to synthesize analogs of an anti-melanoma compound.
J. Comb. Chem. 11(1) , 34-43, (2009) For the successful implementation of Distributed Drug Discovery (D(3)) (outlined in the accompanying Perspective), students, in the course of their educational laboratories, must be able to reproducibly make new, high quality, molecules with potential for bio... |
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Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction.
J. Comb. Chem. 11 , 14-33, (2009) Distributed Drug Discovery (D(3)) proposes solving large drug discovery problems by breaking them into smaller units for processing at multiple sites. A key component of the synthetic and computational stages of D(3) is the global rehearsal of prospective rea... |
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Synthesis of quinazolines and tetrahydroquinazolines: copper-catalyzed tandem reactions of 2-bromobenzyl bromides with aldehydes and aqueous ammonia or amines.
Chem. Asian J. 9(3) , 739-43, (2014) An efficient synthesis of diversely substituted quinazolines and 1,2,3,4-tetrahydroquinazolines through copper-catalyzed tandem reactions of the readily available 2-bromobenzyl bromides, aldehydes, and aqueous ammonia or amines has been developed. By using am... |
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Efficient synthesis of 2-and 3-substituted indenes from 2-bromobenzyl bromide through an enolate alkylation/Cr (II)/Ni (II)-mediated carbonyl addition sequence. Halterman RLand Zhu C.
Tetrahedron Lett. 40(42) , 7445-48, (1999)
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Synthesis and structural studies of tris-2-chlorobenzylamine and tris-2-bromobenzylamine. Chen Q, , et al.
J. Chem. Crystallogr. 35(3) , 177-181, (2005)
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