197335
Triisopropyl borate
≥98%
Synonym(s):
Boric acid triisopropyl ester, Boron isopropoxide, Triisopropoxyborane
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About This Item
Linear Formula:
[(CH3)2CHO]3B
CAS Number:
Molecular Weight:
188.07
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-529-9
Beilstein/REAXYS Number:
1701469
MDL number:
Assay:
≥98%
Form:
liquid
vapor pressure
76 mmHg ( 75 °C)
Quality Level
assay
≥98%
form
liquid
impurities
1% isopropanol
refractive index
n20/D 1.376 (lit.)
bp
139-141 °C (lit.)
density
0.815 g/mL at 25 °C (lit.)
SMILES string
CC(C)OB(OC(C)C)OC(C)C
InChI
1S/C9H21BO3/c1-7(2)11-10(12-8(3)4)13-9(5)6/h7-9H,1-6H3
InChI key
NHDIQVFFNDKAQU-UHFFFAOYSA-N
General description
Trialkyl borate with good thermal properties.
Application
Reagent used to ortho-borylate 1-substituted naphthalenes for Pd-catalyzed coupling with aryl halides.
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signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
62.6 °F - closed cup
flash_point_c
17 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Synthesis, 3478-3478 (2006)
Tetrahedron, 60, 4887-4893 (2004)
Yersica Rios Yepes et al.
Dalton transactions (Cambridge, England : 2003), 49(4), 1124-1134 (2020-01-03)
A set of alkyl aluminum complexes supported by non-symmetric ferrocenyl amidine ligands were used as catalysts for the preparation of cyclic carbonates from epoxides and carbon dioxide using Bu4NI as a co-catalyst. A modified method for the synthesis of aminoferrocene
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 197335-750G | 04061838762412 |
| 197335-2KG | 04061833544983 |
| 197335-80G | 04061838762429 |