Antineoplastic agents

For updated SDS information please visit www.goodfellow.

For updated SDS information please visit www.goodfellow.

For updated SDS information please visit www.goodfellow.

CAS: 7440-42-8 EC No: 231-151-2 MDL No: MFCD00134034 RTECS: ED7350000 UN No: UN3178 Haz Class: 4.1 Packing Group: III Powder Molecular Formula: B MW: 10.81 Melting Point: 2076&deg Boiling Point: 3927&deg Density (g/mL): 2.34

CAS: 7440-42-8 EC No: 231-151-2 MDL No: MFCD00134034 RTECS: ED7350000 UN No: UN3178 Haz Class: 4.1 Packing Group: III Powder Molecular Formula: B MW: 10.81 Melting Point: 2076&deg Boiling Point: 3927&deg Density (g/mL): 2.34

Application Reactant for preparation of: Drug intermediate 6-nitro-L-DOPA Luminescent polystyrene derivatives with sterically protected carbazolylborane moieties High-quality boron-doped graphene via Wurtz-type reductive coupling reaction

Application Reactant for preparation of: Drug intermediate 6-nitro-L-DOPA Luminescent polystyrene derivatives with sterically protected carbazolylborane moieties High-quality boron-doped graphene via Wurtz-type reductive coupling reaction

Application Reactant for preparation of: Drug intermediate 6-nitro-L-DOPA Luminescent polystyrene derivatives with sterically protected carbazolylborane moieties High-quality boron-doped graphene via Wurtz-type reductive coupling reaction

Application Reactant for preparation of: Drug intermediate 6-nitro-L-DOPA Luminescent polystyrene derivatives with sterically protected carbazolylborane moieties High-quality boron-doped graphene via Wurtz-type reductive coupling reaction

Boron tribromide (BBr 3 ) is a strong Lewis acid generally used as a reagent for the deprotection of ethers. Alkyl aryl ethers are cleaved at the alkyl-oxygen bond to give ArOH and alkyl bromides.

Boron tribromide (BBr 3 ) is a strong Lewis acid generally used as a reagent for the deprotection of ethers. Alkyl aryl ethers are cleaved at the alkyl-oxygen bond to give ArOH and alkyl bromides.

Boron tribromide (BBr 3 ) is a strong Lewis acid generally used as a reagent for the deprotection of ethers. Alkyl aryl ethers are cleaved at the alkyl-oxygen bond to give ArOH and alkyl bromides.