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关于此项目
经验公式(希尔记法):
C4H11BLiN
化学文摘社编号:
分子量:
90.89
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
InChI
1S/C4H11BN.Li/c5-6-3-1-2-4-6;/h1-4H2,5H3;/q-1;+1
SMILES string
[Li+].[H][B-]([H])([H])N1CCCC1
InChI key
CUBZYJJJUFGOBJ-UHFFFAOYSA-N
reaction suitability
reagent type: reductant
concentration
1 M in THF
refractive index
n20/D 1.425
density
0.890 g/mL at 25 °C
storage temp.
2-8°C
Application
在与卤代吡啶类化合物和伯烷基甲磺酸酯类化合物反应的情况下,LAB 可以转移胺部分。
能够还原各种官能团。
Lithium Aminoborohydride (LAB) Reagents
- Reducing agent for reduction of carbonic and carboxylic acid derivatives
- Reagent for reduction-amination reactions
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Respiratory system
supp_hazards
存储类别
4.3 - Hazardous materials which set free flammable gases upon contact with water
wgk
WGK 3
flash_point_f
1.4 °F - closed cup
flash_point_c
-17.0 °C - closed cup
法规信息
危险化学品
此项目有
Saikia, P.P.
Synlett, 995-995 (2007)
Fisher, G. B. et al
The Journal of Organic Chemistry, 59, 6378-6378 (1994)
Pasumansky, L. et al
Aldrichimica Acta, 38, 61-61 (2005)
S Thomas et al.
Organic letters, 3(24), 3915-3918 (2001-11-27)
Lithium aminoborohydride (LAB) reagents initiate the amination or reduction of alkyl methanesulfonate esters, as dictated by reaction conditions. Alkyl methanesulfonate esters treated with unhindered LABs provide tertiary amines in excellent yield. Reduction to the corresponding alkane is achieved using a
Shannon Thomas et al.
Organic letters, 5(21), 3867-3870 (2003-10-11)
[reaction: see text] Lithium aminoborohydride (LAB) reagents promote the amination of 2-fluoropyridine under mild reaction conditions, providing 2-(dialkylamino)pyridines in excellent yield and purity. Treatment of 2-fluoropyridine with 1.1 equiv of lithium aminoborohydride at room temperature affords complete conversion after 1
商品
Lithium aminoborohydride (LAB) reagents are a new class of powerful and selective reagents developed in the laboratory of Professor Bakthan Singaram at the University of California, Santa Cruz.
相关内容
New asymmetric methodology meets the continuous demand for optically active compounds in various fields.
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