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About This Item
線性公式:
BBr3 · S(CH3)2
CAS號碼:
分子量：:
312.66
MDL號碼:
分類程式碼代碼:
12352101
PubChem物質ID:
NACRES:
NA.22
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推薦產品
化驗
97%
形狀
powder
mp
106-108 °C (lit.)
官能基
thioether
SMILES 字串
C[S+](C)[B-](Br)(Br)Br
InChI
1S/C2H6BBr3S/c1-7(2)3(4,5)6/h1-2H3
InChI 密鑰
NCVLHAUANAMSTL-UHFFFAOYSA-N
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應用
Boron tribromide dimethyl sulfide complex (BBr3S(CH3)2) can be used as a reagent:
- To deprotect the methylenedioxy acetal bonding of poly vinyl-1, 3-benzodioxole.[1]
- To prepare benzyl S,S′-diphenyl acetal by reacting with carboxylic acid and thexylphenylthioborane.[2]
- To prepare Baylis-Hillman adducts by the reaction of aldehydes with 3-buten-2-one.[3]
Boron tribromide in convenient solid form. Used as a brominating agent.[4]
Reactant for preparation of:
Reagent for:
- Precursor of HIV protease inhibitor KNI 764 using cation-exchange resin mediated Mannich reaction
Reagent for:
- Baylis-Hillman reactions
訊號詞
Danger
危險聲明
危險分類
Skin Corr. 1B
安全危害
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類（WGK）
WGK 3
個人防護裝備
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
客戶也查看了
Protection and Polymerization of Functional Monomers. 24. Anionic Living Polymerizations of 5-Vinyl-and 4-Vinyl-1, 3-benzodioxoles
Ishizone T, et al.
Macromolecules, 28(11), 3787-3793 (1995)
Inorganic Chemistry, 29, 4162-4162 (1990)
Dimethyl sulfide-boron trihalide-mediated reactions of α, β, unsaturated ketones with aldehydes: one-pot synthesis of Baylis-Hillman adducts and ?-halomethyl enones
Iwamura T, et al.
Tetrahedron, 57(40), 8455-8462 (2001)
Direct conversion of carboxylic acids and carboxylic esters into S, S?-diphenyl acetals and phenyl sulfides with thexylphenylthioborane
Kim S and Kim SS
Tetrahedron Letters, 28(17), 1913-1916 (1987)
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