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Merck
CN

307408

Lithium diisopropylamide mono(tetrahydrofuran) solution

1.5 M in cyclohexane

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About This Item

Empirical Formula (Hill Notation):
C10H22LiNO
CAS Number:
Molecular Weight:
179.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Concentration:
1.5 M in cyclohexane
Form:
liquid
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InChI

1S/C6H14N.C4H8O.Li/c1-5(2)7-6(3)4;1-2-4-5-3-1;/h5-6H,1-4H3;1-4H2;/q-1;;+1

SMILES string

[Li+].C1CCOC1.CC(C)[N-]C(C)C

InChI key

YTJXGDYAEOTOCG-UHFFFAOYSA-N

vapor density

>1 (vs air)

form

liquid

concentration

1.5 M in cyclohexane

density

0.816 g/mL at 25 °C

storage temp.

2-8°C

Application

Lithium diisopropylamide mono(tetrahydrofuran) can be used:
  • As an initiator in the anionic polymerization of D,L-lactide.
  • In one of the key synthetic steps for the preparation of phenylacetic acid component of muscarinic M3 receptor antagonist.
  • In the synthesis of new sexithiophene derivatives, which are used as electron donor materials in bilayer photovoltaic devices.

Other Notes

may contain a small amount of THF and ethylbenzene

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT RE 2 - STOT SE 3

target_organs

Central nervous system, hearing organs

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

-0.4 °F - closed cup

flash_point_c

-18 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Synthesis and properties of end-capped sexithiophenes incorporating the ethylene dithiothiophene unit
Mason CR, et al.
Journal of Materials Chemistry, 15(14), 1446-1453 (2005)
Diastereoselective synthesis of the acid part of a new muscarinic M3 receptor antagonist
Mitsuya M, et al.
Tetrahedron, 56(51), 9901-9907 (2000)
Anionic polymerization of D, L-lactide initiated by lithium diisopropylamide
Bhaw-Luximon A, et al.
Polymer, 42(24), 9651-9656 (2001)

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