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Organolithium

Organolithium compounds possess direct bonds between carbon and lithium atoms. Organolithium reagents are strongly basic, highly reactive nucleophiles used to transfer organic groups or lithium atoms to substrates during organic synthesis reactions.
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Keyword Search:
1 – 15 of 150 results
1

Lithium salicylate, tech.

CAS: 552-38-5 Molecular Formula: C7H5LiO3 Molecular Weight (g/mol): 144.054 MDL Number: MFCD00045813 InChI Key: PSBOOKLOXQFNPZ-UHFFFAOYSA-M Synonym: lithium salicylate,unii-93f1sp6qin,salicylic acid lithium salt,dilithium salicylate,93f1sp6qin,lithium 2-hydroxybenzoate,lithium 1+ ion salicylate,lithiumsalicylate,lithiumsalicylat,salicylicacidlithiumsalt PubChem CID: 23663621 IUPAC Name: lithium;2-hydroxybenzoate SMILES: [Li+].C1=CC=C(C(=C1)C(=O)[O-])O

PubChem CID 23663621
CAS 552-38-5
Molecular Weight (g/mol) 144.054
MDL Number MFCD00045813
SMILES [Li+].C1=CC=C(C(=C1)C(=O)[O-])O
Synonym lithium salicylate,unii-93f1sp6qin,salicylic acid lithium salt,dilithium salicylate,93f1sp6qin,lithium 2-hydroxybenzoate,lithium 1+ ion salicylate,lithiumsalicylate,lithiumsalicylat,salicylicacidlithiumsalt
IUPAC Name lithium;2-hydroxybenzoate
InChI Key PSBOOKLOXQFNPZ-UHFFFAOYSA-M
Molecular Formula C7H5LiO3
2

Lithium 2,4-pentanedionate, 99.5%

CAS: 18115-70-3 Molecular Formula: C5H7LiO2 Molecular Weight (g/mol): 106.05 MDL Number: MFCD00013496 InChI Key: JTEOOCAGEXVCBQ-LNKPDPKZSA-M Synonym: Lithium acetylacetonate IUPAC Name: lithium(1+) (2Z)-4-oxopent-2-en-2-olate SMILES: [Li+].C\C([O-])=C\C(C)=O

CAS 18115-70-3
Molecular Weight (g/mol) 106.05
MDL Number MFCD00013496
SMILES [Li+].C\C([O-])=C\C(C)=O
Synonym Lithium acetylacetonate
IUPAC Name lithium(1+) (2Z)-4-oxopent-2-en-2-olate
InChI Key JTEOOCAGEXVCBQ-LNKPDPKZSA-M
Molecular Formula C5H7LiO2
3

Lithium tri-tert-butoxyaluminum hydride, nominally 1M in THF, packaged under Argon in resealable ChemSeal™ bottles

CAS: 17476-04-9 Molecular Formula: C12H28AlLiO3 MDL Number: MFCD00011532 Synonym: Lithium hydridotris(tert-butoxy)aluminate

CAS 17476-04-9
MDL Number MFCD00011532
Synonym Lithium hydridotris(tert-butoxy)aluminate
Molecular Formula C12H28AlLiO3
4

Lithium vanadium oxide, 99.9% (metals basis)

CAS: 15060-59-0 MDL Number: MFCD00053997 Synonym: Lithium vanadate

CAS 15060-59-0
MDL Number MFCD00053997
Synonym Lithium vanadate
5

Lithium niobium isopropoxide, 99+% (metals basis), 5% w/v in isopropanol

CAS: 21864-21-1 Molecular Formula: C18H42LiNbO6 MDL Number: MFCD00210626

CAS 21864-21-1
MDL Number MFCD00210626
Molecular Formula C18H42LiNbO6
6

(2,2,6,6-Tetramethyl-3,5-heptanedionato)lithium, 98%, Thermo Scientific Chemicals

CAS: 22441-13-0 MDL Number: MFCD00142754 Synonym: Lithium 2,2,6,6-tetramethyl-3,5-heptanedionate; Li(TMHD)

CAS 22441-13-0
MDL Number MFCD00142754
Synonym Lithium 2,2,6,6-tetramethyl-3,5-heptanedionate; Li(TMHD)
7

Lithium niobium methoxide, 99+% (metals basis), 5% w/v in methanol

CAS: 21864-11-9 MDL Number: MFCD00210627 Synonym: lithium niobium methoxide

CAS 21864-11-9
MDL Number MFCD00210627
Synonym lithium niobium methoxide
9

Sigma Aldrich Hexyllithium Solution

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

ENCOMPASS ENCOMPASS_PREFERRED
Boiling Point 69°C
Linear Formula CH3(CH2)5Li
CAS 21369-64-2
Biological Activity Central Nervous System, Nervous System
Molecular Weight (g/mol) 92.11 g/mol
MDL Number MFCD00191446
Health Hazard 1 UN 3394 4.3(4.2) / PGI
Recommended Storage 2°C to 8°C
Molecular Formula C6H13Li
Density 0.708 g/mL at 25°C
10

Sigma Aldrich 3-(1,3-Thiazol-4-yl)aniline

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

ENCOMPASS ENCOMPASS_PREFERRED
CAS 134812-28-5
11

Sigma Aldrich 2-Ethoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

ENCOMPASS ENCOMPASS_PREFERRED
CAS 848243-23-2
12

Sigma Aldrich Methyl 3,5-dimethoxybenzoate

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

ENCOMPASS ENCOMPASS_PREFERRED
CAS 2150-37-0
13

Sigma Aldrich Tantalum(V) ethoxide

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

ENCOMPASS ENCOMPASS_PREFERRED
Boiling Point 155°C (0.01 mmHg)
Percent Purity 99.98% trace metals basis
Linear Formula Ta(OC2H5)5
CAS 6074-84-6
Molecular Weight (g/mol) 406.25
MDL Number MFCD00049785
Refractive Index n20/D 1.487 (literature)
Synonym Pentaethoxytantalum; Pentaethyl tantalate; Tantalum ethylate; Tantalum pentaethoxide; Tantalum(V) ethoxide
Recommended Storage Room Temperature
Molecular Formula C10H25O5Ta
Density 1.566 g/mL (at 25°C)
Melting Point 21°C
14

Sigma Aldrich Lithium Bis(trifluoromethanesulfonyl)imide Anhydrous 99.99% Trace Metals Basis

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

ENCOMPASS ENCOMPASS_PREFERRED
Recommended Storage Room Temperature
15

Medchemexpress LLC 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose | 4064-06-6 | MFCD00063225 | 97.0% | 260.28 g·mol⁻¹ | C12H20O6 | 5 G
SDP

1,2:3,4-di-O-isopropylidene-α-D-galactopyranose is an isopropylidene-protected derivative of D-galactopyranose used as an intermediate and reagent in carbohydrate synthesis and organic chemistry. It protects vicinal hydroxyl groups to enable selective transformations, and is used in oligosaccharide synthesis, glycosylation studies, and other carbohydrate-based research.

  • Provides isopropylidene protection of vicinal diols enabling selective reactions.
  • Suitable as a synthetic intermediate for carbohydrate chemistry.
  • Supplied at laboratory research purity for reproducible results (97.0%).
  • Well-defined molecular formula and molecular weight for characterization.
  • Manufacturer documents include datasheet, certificate of analysis, and safety data sheet.

ENCOMPASS_PREFERRED