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Merck

746061

Difluoromethyl 2-pyridyl sulfone

97% (HPLC)

동의어(들):

2-[(Difluoromethyl)sulfonyl]pyridine, Hu Reagent, 2-(Difluoromethylsulfonyl)pyridine, 2-PySO2CF2H

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크기 선택

1 G

₩170,926

5 G

₩799,719

₩170,926


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제품정보 (DICE 배송 시 비용 별도)

실험식(Hill 표기법):
C6H5F2NO2S
CAS 번호:
Molecular Weight:
193.17
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
20317604

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제품 이름

Difluoromethyl 2-pyridyl sulfone, 97% (HPLC)

InChI

1S/C6H5F2NO2S/c7-6(8)12(10,11)5-3-1-2-4-9-5/h1-4,6H

SMILES string

O=S(C1=CC=CC=N1)(C(F)F)=O

InChI key

YRQNSTAWTLXCEZ-UHFFFAOYSA-N

assay

97% (HPLC)

form

solid

mp

44-49 °C

functional group

fluoro
sulfone

Quality Level

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유사한 품목 비교

전체 비교 보기

차이점 표시

1 of 4

이 품목
403636442801392960
assay

97% (HPLC)

assay

96%

assay

97%

assay

97%

form

solid

form

solid

form

-

form

solid

mp

44-49 °C

mp

40-42 °C (lit.)

mp

145-149 °C (lit.)

mp

82-84 °C (dec.) (lit.)

functional group

fluoro

functional group

fluoro

functional group

fluoro

functional group

phosphine

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

Application

Reagent is used in the olefination of ketones and aldehydes to form gem-difluoro olefins under basic conditions.[1] Product is also used as a crucial intermediate toward making 1,1-difluorinated alkyl chains for the alkylation of heterocycles.[2]

General description

Difluoromethyl 2-pyridyl sulfone (2-PySO2CF2H) is a reagent used in the gem-difluoroolefination of aldehydes and ketones. It is also used as a reagent in the nucleophilic difluoro(sulfonato)methylation of alcohols, N-sulfinyl imines, and halides.[3][4]

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2

저장 등급

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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문서 라이브러리 방문

Difluoromethyl 2?Pyridyl Sulfone
e-EROS Encyclopedia of Reagents for Organic Synthesis (2016)
Difluoromethyl 2?Pyridyl Sulfone
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2016)
Difluoromethyl 2-pyridyl sulfone: a versatile carbonyl gem-difluoroolefination reagent
Gao B, et al.
Organic Chemistry Frontiers : An International Journal of Organic Chemistry / Royal Society of Chemistry, 2(2), 163-168 (2015)
From difluoromethyl 2-pyridyl sulfone to difluorinated sulfonates: a protocol for nucleophilic difluoro(sulfonato)methylation.
G K Surya Prakash et al.
Angewandte Chemie (International ed. in English), 50(11), 2559-2563 (2011-03-04)
Yanchuan Zhao et al.
Organic letters, 12(7), 1444-1447 (2010-03-10)
Difluoromethyl 2-pyridyl sulfone, a previously unknown compound, was found to act as a novel and efficient gem-difluoroolefination reagent for both aldehydes and ketones. It was found that the fluorinated sulfinate intermediate in the reaction is relatively stable, which can be

관련 콘텐츠

Prof. Jinbo Hu's lab focuses on developing new fluorination reagents and reactions, including difluoromethylation and monofluoromethylation.

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활성 필터

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

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