| Chemical Name | Boron tribromide |
| Synonym |
BORON TRIBROMIDE, REAGENTPLUS, >=99%
BORON TRIBROMIDE, 99.995%
晶碱石
boron (III) bromide
BORON TRIBROMIDE, REAGENTPLUS, 99.9%
Bortribromid
三溴化硼(0402禁空运)
boronbromide(bbr3)
三溴化硼,1M在二氯甲烷溶剂中
Boron tribromide
tribromoborane
三溴化硼
BORON TRIBROMIDE, 1.0M SOLUTION IN HEPTA NE
tribromo-boran
Boron bromide (BBr3)
BORON TRIBROMIDE SOLUTION, ~1 M IN DICHL OROMETHANE
Borane,tribromo-
Boron,tribromo-
trona
天然碱
BORON TRIBROMIDE
BBr3
三溴化硼 溶液
Borane, tribromo-
BORON TRIBROMIDE, 1.0M SOLUTION IN HEXAN ES
Tribromoboron
tribromuredebore
溴化硼
boron tribromide
三溴硼烷(爆炸,禁止销售)BORON TRIBROMIDE, 99.9%
三溴硼烷
丝光晶碱石
BORON TRIBROMIDE, 1.0M SOLUTION IN DICHL OROMETHANE
Boron tribromide Solution
BORON BROMIDE
Boron bromide
溴化硼;天然碱
三溴化硼, 99% MIN
碳酸钠石
tribromoboron
Tribromoborane
天然碱;碳酸钠石
BBr3 |
| CAS Number | 10294-33-4 |
| PubChem Substance ID | 125307031 |
| EC Number | 233-657-9 |
| MDL Number | MFCD00011312 |
| Reaxys-RN | 3903058 |
| Merck Number | 1347 |
| Beilstein Registry Number | 2384789 |
| Chemical Name Translation | 三溴化硼 |
| LabNetwork Molecule ID | LN00163667 |
⑴.易被水和醇等分解,受热会爆炸,对人体组织有强烈刺激作用,其蒸气剧毒,腐蚀性较强,具有强吸水性,见光、遇热易分解,接触空气冒白烟。为强路易式酸,能与碱反应形成络合物和加成物。
⑵.在干燥空气中不变化。溶于无机酸并剧烈起泡。天然碱产于不同的盐湖沉积物中,主要产于碱湖及古代沉积矿床中,常与针碳钠钙石、水碱、泡碱、石盐、芒硝、钙芒硝、无水芒硝和石膏共生。遇空气中的湿气很容易水解。
⑶.重要的工业原料,广泛用于玻璃、化工、轻工、纺织、漂染、冶金、石油加工、医药、食品等方面。
⑷.用作半导体的掺杂材料,有机
用作有机合成的催化剂、中间体和溴化剂,制造高纯硼及其它有机硼化合物的原料。
{ALF} Reagent for cleavage of ethers: Synthesis, 249 (1983). Converts alcohols to alkyl bromides under mild conditions: Tetrahedron Lett., 35, 1051 (1994). Cleavage of N-methoxymethyl: Tetrahedron Lett., 42, 8633 (2001), or N-benzyl: Tetrahedron Lett., 45, 4093 (2004) protecting groups can also be achieved under mild conditions. Alkynes undergo bromoboration; the products can be transformed, e.g. to trisubstituted alkenes: Tetrahedron Lett., 29, 1811 (1988), or enyne-allenes: Tetrahedron Lett., 35, 1829 (1994).
{uni_hamburg} Short: II/25A
{ALD} Merck:14,1347
{ALF} Reagent for cleavage of ethers. For a brief feature of uses of the reagent in organic synthesis, see: Synlett, 1636 (2005). See also preceding entry.
{ALF} Reagent for cleavage of ethers: Synthesis, 249 (1983). Converts alcohols to alkyl bromides under mild conditions: Tetrahedron Lett., 35, 1051 (1994). Cl