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659274

Sigma-Aldrich

Potassium allyltrifluoroborate

95%

Synonym(s):

Potassium trifluoro(prop-2-enyl)borate

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About This Item

Empirical Formula (Hill Notation):
C3H5BF3K
CAS Number:
233664-53-4
Molecular Weight:
147.98
MDL number:
MFCD07368222
UNSPSC Code:
12352103
PubChem Substance ID:
24884410
NACRES:
NA.22

Quality Level

100

Assay

95%

form

solid

mp

>300 °C

SMILES string

[K+].F[B-](F)(F)CC=C

InChI

1S/C3H5BF3.K/c1-2-3-4(5,6)7;/h2H,1,3H2;/q-1;+1

InChI key

TVPZAMJXLCDMIT-UHFFFAOYSA-N

Related Categories

Application

Organotrifluoroborate involved in:
  • Catalytic allylboration
  • Stereoselective nucleophilic addition
  • Pd-catalyzed heterocyclizations
  • Oxidation reactions and Oxidative Mannich reactions
  • Cross-coupling reactions

Organotrifluoroborates as versatile and stable boronic acid surrogates.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H315,H318,H335

Hazard Classifications

Eye Dam. 1 - 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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

659274-VAR:
659274-1G:
659274-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
SHBJ6412
SHBF0655V
10331AE

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Articles

Potassium Organotrifluoroborates

These bench stable Potassium Organotrifluoroborates are useful for Suzuki-Miyaura cross-coupling reactions and have also been used for a variety of other C-C bond forming reactions. Importantly, these reagents are compatible with a wide range of functional groups and are stable to many commonly used and harsh reaction conditions.

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