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Merck
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328103

Sigma-Aldrich

3′-Hydroxyacetophenone

≥99%

동의어(들):

1-(3-Hydroxyphenyl)ethanone, 3-Acetylphenol, 3-Hydroxyphenylethanone, m-Hydroxyacetophenone

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크기 선택

5 G
₩30,450
25 G
₩48,619

₩30,450

구입 가능 여부는 고객센터에 문의하십시오.
벌크 견적 요청
모든 사진(1)

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보기 변경
5 G
₩30,450
25 G
₩48,619

About This Item

Linear Formula:
HOC6H4COCH3
CAS Number:
121-71-1
Molecular Weight:
136.15
Beilstein:
2040676
EC Number:
204-494-0
MDL number:
MFCD00002298
UNSPSC 코드:
12352100
PubChem Substance ID:
24859714
NACRES:
NA.22

₩30,450

구입 가능 여부는 고객센터에 문의하십시오.
벌크 견적 요청

분석

≥99%

bp

296 °C (lit.)

mp

90-95 °C (lit.)

density

1.1 g/mL at 25 °C (lit.)

작용기

ketone

SMILES string

CC(=O)c1cccc(O)c1

InChI

1S/C8H8O2/c1-6(9)7-3-2-4-8(10)5-7/h2-5,10H,1H3

InChI key

LUJMEECXHPYQOF-UHFFFAOYSA-N

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일반 설명

3′-Hydroxyacetophenone is an hydroxy-substituted alkyl phenyl ketone.[1]

애플리케이션

3′-Hydroxyacetophenone was used in synthesis of enantiopure (-)-rivastigmine.[2] It was also used in preparation of building block for synthesis of dendritic compounds.[3]

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

247.3 °F - closed cup

Flash Point (°C)

119.6 °C - closed cup

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves

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시험 성적서(COA)

Lot/Batch Number
WXBC8212V
SHBK2858
SHBH0449V
SHBB9189V
57196PKV

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문서 라이브러리 방문

Kiwon Han et al.
The Journal of organic chemistry, 75(9), 3105-3108 (2010-03-30)
A practical and efficient procedure for the synthesis of rivastigmine was developed. This procedure includes dynamic kinetic resolution using a polymer-bound ruthenium complex and a lipase in combination as a key step. Enantiopure (-)-rivastigmine was obtained from commercially available 3'-hydroxyacetophenone
Katharine Moore Tibbetts et al.
The journal of physical chemistry. A, 118(37), 8170-8176 (2014-03-01)
The hydroxy-substituted alkyl phenyl ketones 2'-, 3'- and 4'- (ortho, meta, and para) hydroxyacetophenone were excited in the strong-field regime with wavelengths ranging from 1200-1500 nm to produce the respective radical cations. For 2'- and 3'-hydroxyacetophenone, the parent molecular ion
Synthesis of polyester dendrimers and dendrons starting from Michael reaction of acrylates with 3-hydroxyacetophenone.
Hirayama Y, et a
Tetrahedron Letters, 46(6), 1027-1030 (2005)
Takashi Otani et al.
Bioorganic & medicinal chemistry letters, 18(12), 3582-3584 (2008-05-31)
m-Acetylphenyl-beta-d-glucopyranosides and m-acetylphenyl-alpha/beta-d-mannopyranosides were synthesized by the Koenigs-Knorr, Mitsunobu, and Helferich reactions as key glycosylation reactions, respectively. Their spectroscopic properties and antioxidative activities were characterized as potential ultraviolet B-ray absorbents.
Stefania Ferrari et al.
Journal of medicinal chemistry, 54(1), 211-221 (2010-12-04)
Folate analogue inhibitors of Leishmania major pteridine reductase (PTR1) are potential antiparasitic drug candidates for combined therapy with dihydrofolate reductase (DHFR) inhibitors. To identify new molecules with specificity for PTR1, we carried out a virtual screening of the Available Chemicals
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