Skip to Content
Merck
All Photos(1)

Key Documents

718947

Sigma-Aldrich

Potassium (iodomethyl)trifluoroborate

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
CH2BF3IK
CAS Number:
Molecular Weight:
247.84
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

form

solid

mp

245-258 °C (dec.)

functional group

iodo

SMILES string

[K+].C[B-](C)(C)CI

InChI

1S/C4H11BI.K/c1-5(2,3)4-6;/h4H2,1-3H3;/q-1;+1

InChI key

YPGDEVDDTXBNRH-UHFFFAOYSA-N

Related Categories

Application

Organotrifluoroborate involved in synthesis of functionalized ethyltrifluoroborates

Organotrifluoroboronates as versatile and stable boronic acid surrogates.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

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


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Articles

Bench-stable Potassium Organotrifluoroborates enable diverse C-C bond formation reactions.

Bench-stable Potassium Organotrifluoroborates enable diverse C-C bond formation reactions.

Bench-stable Potassium Organotrifluoroborates enable diverse C-C bond formation reactions.

Bench-stable Potassium Organotrifluoroborates enable diverse C-C bond formation reactions.

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

Contact Technical Service