906298

3-(4-Bromophenyl)-3-(trifluoromethyl)-3H-diazirine

Manufacturer: Sigma Aldrich

CAS Number: 952143-02-1

Synonym(S): Probe building block for photoaffinity labeling, Suzuki-Miyaura-compatible multifunctional photo probe building block, Trifluoromethyl diazirine aryl bromide

Select a Size

Pack Size SKU Availability Price
50 MG 906298-50-MG In Stock ₹ 22,440.23

906298 - 50 MG

₹ 22,440.23

In Stock

Quantity

1

Base Price: ₹ 22,440.23

GST (18%): ₹ 4,039.241

Total Price: ₹ 26,479.471

Assay

≥95%

form

liquid

reaction suitability

reagent type: cross-linking reagent

storage temp.

2-8°C

SMILES string

BrC1=CC=C(C2(N=N2)C(F)(F)F)C=C1

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Description

  • Application: 3-(4-Bromophenyl)-3-(trifluoromethyl)-3H-diazirine is a Suzuki-Miyaura (S−M)-compatible building block tailored for the design of photoaffinity probes (PAPs). Photoaffinity labeling (PAL) is of growing interest in chemical biology and drug discovery research for use in protein profiling; covalent inhibitors; protein-protein interactions and complexes; and target engagement, identification, or validation studies. Diazirines are desirable photoactivable groups for chemical probes; however, their installation is not always straightforward. In response, diazirine-tolerant S-M coupling conditions were developed by Ichiishi, et al, using 3-(4-bromophenyl)-3-(trifluoromethyl)-3H-diazirine and shown to be efficient and scalable with minimal perturbation of the diazirine.Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)
  • Other Notes: Reducing Limitation in Probe Design: The Development of a Diazirine-Compatible Suzuki-Miyaura Cross Coupling Reaction

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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≥95%

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reagent type: cross-linking reagent

storage temp.:
2-8°C

SMILES string:
BrC1=CC=C(C2(N=N2)C(F)(F)F)C=C1

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Assay:
≥99% (HPLC)

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powder

reaction suitability:
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storage temp.:
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SMILES string:
CCC(CCCC)CN1C2=CC(N(C3=CC=C(OC)C=C3)C4=CC=C(OC)C=C4)=CC=C2C5=CC=C(N(C6=CC=C(OC)C=C6)C7=CC=C(OC)C=C7)C=C15