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ALD00484

Sigma-Aldrich

Sodium 7-Chloro-1,1-difluoroheptane-1-sulfinate

contains ≤15% sodium 7-(ethylthio)-1,1-difluoroheptane-1-sulfinate

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About This Item

Empirical Formula (Hill Notation):
C7H12ClF2NaO2S
Molecular Weight:
256.67
UNSPSC Code:
12352101
PubChem Substance ID:
329772692
NACRES:
NA.22

form

powder

Quality Level

100

contains

≤15% sodium 7-(ethylthio)-1,1-difluoroheptane-1-sulfinate

reaction suitability

reaction type: C-C Bond Formation
reaction type: C-H Activation
reagent type: catalyst

mp

185 °C

SMILES string

O=S(C(F)(F)CCCCCCCl)O[Na]

InChI

1S/C7H13ClF2O2S.Na/c8-6-4-2-1-3-5-7(9,10)13(11)12;/h1-6H2,(H,11,12);/q;+1/p-1

InChI key

LFIQXRUQAPPIPD-UHFFFAOYSA-M

Application

The following Baran Sulfinate is a part of a toolbox of diversification reagents, which are ideal for the late-stage functionalization of nitrogen-containing heterocycles. The regioselectivity can be effectively tuned by modification of the pH and solvent selection.

Other Notes

Radical-Based Regioselective C–H Functionalization of Electron-Deficient Heteroarenes: Scope, Tunability, and Predictability

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKBX5823V

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Articles

Baran Diversinates™

The synthesis of heteroaromatic and aromatic compounds is at the heart of the chemical industry. The ever-growing demand for new chemical entities, coupled with dwindling resources and time constraints allotted to any given research project, a rapid way to diversify (hetero)aromatic scaffolds is needed.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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