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3,5-bis-(Trifluoromethyl)acetophenone CAS 30071-93-3

3,5-bis-(Trifluoromethyl)acetophenone CAS 30071-93-3

3,5-bis-(Trifluoromethyl)acetophenone
CAS 30071-93-3
Purity: 98.0%Min | Appearance: Pale yellow solid
Molecular Formula: C10H4F6O | MW: 256.145
Einecs: 250-023-7
Synonyms: 1-(3,5-bis(trifluoromethyl)phenyl)ethan-1-one;1-[3,5-bis(trifluoromethyl)phenyl]ethanone;3',5'-bis(trifluoromethyl)acetophenone

Product Introduction

Dayang Chem (Hangzhou) Co., Ltd. is one of the leading manufacturers and suppliers of 3,5-bis-(trifluoromethyl)acetophenone cas 30071-93-3 in China, specialized in providing high quality customized chemicals. Welcome to wholesale bulk 3,5-bis-(trifluoromethyl)acetophenone cas 30071-93-3 made in China here and get pricelist from our factory. Good service and reasonable price are available.

 

Product Introduction:

 

1.     Specification

Appearance

Pale yellow solid

Assay

98.0% Min

Loss on Drying

1.0% Max

 

The latest specifications and COA will be sent upon request.

 

2.     Packaging & shipping

Packaging

R&D Sample Sizes: 1 g, 10 g, 100 g and 1kg bottle or aluminum bag for laboratory evaluation.

Transport Classification

Not regulated as a dangerous good

Lead Time

in stock

Shipping Methods

DHL, FedEx, air freight or sea freight

f-35-bis-Trifluoromethylacetophenone

s-35-bis-Trifluoromethylacetophenone

 

3.     Applications

Key building blocks in multi-step organic synthesis for pharmaceuticals and fine chemicals.

 

4.     Spectrum

t-30071-93-3-35-bis-Trifluoromethylacetophenone

 

5.     Related Articles

1. Inhibition of monoamine oxidase-B by 5H-indeno[1,2-c]pyridazines: biological activities, quantitative structure-activity relationships (QSARs) and 3D-QSARs.J. Med. Chem.   38 , 3874-83, (1995)
2. Asymmetric biocatalytic reduction of 3,5-bis(trifluoromethyl) acetophenone to (1R)-[3,5-bis(trifluoromethyl)phenyl] ethanol using whole cells of newly isolated Leifsonia xyli HS0904.Appl. Microbiol. Biotechnol.   90(6) , 1897-904, (2011)
3. Rhodium-catalyzed heterogeneous enantioselective hydrogenation of 3, 5-di-(trifluoromethyl)-acetophenone. Hess R, et al.J. Mol. Catal. A: Chem.   212(1) , 205-9, (2004)

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