121-71-1

  • Product Name:3-Hydroxyacetophenone
  • Molecular Formula:C8H8O2
  • Purity:99%
  • Molecular Weight:136.15
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Product Details;

CasNo: 121-71-1

Molecular Formula: C8H8O2

Appearance: white crystal powder

Buy Reliable Quality Hot Sale 3-Hydroxyacetophenone 121-71-1 Efficient Delivery

  • Molecular Formula:C8H8O2
  • Molecular Weight:136.15
  • Appearance/Colour:white crystal powder 
  • Vapor Pressure:0.022Pa at 25℃ 
  • Melting Point:90-95 °C(lit.) 
  • Refractive Index:1,534 
  • Boiling Point:277 °C at 760 mmHg 
  • PKA:9.19(at 25℃) 
  • Flash Point:115.8 °C 
  • PSA:37.30000 
  • Density:1.10 g/cm3 
  • LogP:1.59480 

3'-Hydroxyacetophenone(Cas 121-71-1) Usage

Description

3’-Hydroxyacetophenone is a chemical compound and it is a component of castoreum, the exudate from the castor sacs of the mature beaver. It is used in the synthesis and preparation of chalcones and flavonoids as anti-tuberculosis agents, as well as antileishmanial chaocones.

Chemical Properties

beige-brown crystalline powder

Uses

3’Hydroxyacetophenone is a chemical reagent used in the synthesis and preparation of chalcones and flavonoids as anti-tuberculosis agents, as well as antileishmanial chaocones.

Preparation

Preparation by diazotization of 3-aminoacetophenone, followed by hydrolysis of the obtained diazonium salt (78–82%).

General Description

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

Flammability and Explosibility

Nonflammable

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

121-71-1 Relevant articles

Preparation and trapping of 3-lithium-O-lithiophenoxide

Selnick,Bourgeois,Butcher,Radzilowski

, p. 2043 - 2046 (1993)

3-Bromophenol and 3-bromothiophenol are ...

Palladium(II)-catalyzed aerobic hydroalkoxylation of styrenes containing a phenol

Gligorich, Keith M.,Schultz, Mitchell J.,Sigman, Matthew S.

, p. 2794 - 2795 (2006)

An intermolecular Pd-catalyzed hydroalko...

Efficient microwave-assisted Pd-catalyzed hydroxylation of aryl chlorides in the presence of carbonate

Yu, Chao-Wu,Chen, Grace S.,Huang, Chen-Wei,Chern, Ji-Wang

, p. 3688 - 3691 (2012)

An efficient microwave-assisted, palladi...

Nickel-catalyzed deallylation of aryl allyl ethers with hydrosilanes

Ding, Guangni,Fan, Sijie,Wang, Jingyang,Wang, Yu,Wu, Xiaoyu,Xie, Xiaomin,Yang, Liqun,Zhang, Zhaoguo

supporting information, (2021/09/28)

An efficient and mild catalytic deallyla...

Aryl phenol compound as well as synthesis method and application thereof

-

Paragraph 0100-0102, (2021/05/12)

The invention discloses a synthesis meth...

Iron-catalyzed domino decarboxylation-oxidation of α,β-unsaturated carboxylic acids enabled aldehyde C-H methylation

Gong, Pei-Xue,Xu, Fangning,Cheng, Lu,Gong, Xu,Zhang, Jie,Gu, Wei-Jin,Han, Wei

supporting information, p. 5905 - 5908 (2021/06/18)

A practical and general iron-catalyzed d...

Iron-catalyzed arene C-H hydroxylation

Cheng, Lu,Wang, Huihui,Cai, Hengrui,Zhang, Jie,Gong, Xu,Han, Wei

, p. 77 - 81 (2021/10/05)

The sustainable, undirected, and selecti...

121-71-1 Process route

ketoprofen
22071-15-4,22161-86-0

ketoprofen

hydratropic acid
492-37-5,2328-24-7

hydratropic acid

3-Hydroxyacetophenone
121-71-1

3-Hydroxyacetophenone

2-(m-hydroxyphenyl)propionic acid
56911-50-3

2-(m-hydroxyphenyl)propionic acid

C<sub>16</sub>H<sub>13</sub>NO<sub>5</sub>

C16H13NO5

(+/-)-2-<3-(3-hydroxybenzoyl)phenyl>propanoic acid

(+/-)-2-<3-(3-hydroxybenzoyl)phenyl>propanoic acid

Conditions
Conditions Yield
With sodium nitrate; water; ozone; tert-butyl alcohol; Kinetics;
 
C<sub>20</sub>H<sub>19</sub>NO<sub>9</sub>S

C20H19NO9S

3-Hydroxyacetophenone
121-71-1

3-Hydroxyacetophenone

sulfanilamide
63-74-1

sulfanilamide

Conditions
Conditions Yield
C20H19NO9S; With hydrogenchloride; In water; for 8h; Reflux;
With ammonium hydroxide; for 3h; Further stages; Reflux;
606 g
697 g

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