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METHYL 4-METHOXYPHENYLACETATE

Basic Information

  • CAS No.: 23786-14-3

Physical properties

Product Description

METHYL 4-METHOXYPHENYLACETATE GMP Manufacturer Global Trade 23786-14-3 with Fast Delivery

  • Molecular Formula: C10H12O3
  • Molecular Weight: 180.203
  • Appearance/Colour: clear colorless to yellow liquid 
  • Vapor Pressure: 0.000151mmHg at 25°C 
  • Refractive Index: n20/D 1.516(lit.)  
  • Boiling Point: 264 °C at 760 mmHg 
  • Flash Point: 100.4 °C 
  • PSA: 35.53000 
  • Density: 1.083 g/cm3 
  • LogP: 1.41070 

METHYL 4-METHOXYPHENYLACETATE(Cas 23786-14-3) Usage

InChI:InChI=1/C10H12O4/c1-13-8-5-3-7(4-6-8)9(11)10(12)14-2/h3-6,9,11H,1-2H3

23786-14-3 Relevant articles

SUBSTITUTED PIPERAZINE DERIVATIVES USEFUL AS T CELL ACTIVATORS

-

Page/Page column 103, (2021/07/02)

Disclosed are compounds of Formula (I): ...

syn-Selective Michael Reaction of α-Branched Aryl Acetaldehydes with Nitroolefins Promoted by Squaric Amino Acid Derived Bifunctional Br?nsted Bases

Campano, Teresa E.,García-Urricelqui, Ane,Mielgo, Antonia,Palomo, Claudio,de Cózar, Abel

supporting information, p. 3604 - 3612 (2021/07/26)

Here we describe a direct access to 2,2,...

B(C6F5)3-catalyzed O-H insertion reactions of diazoalkanes with phosphinic acids

Jiang, Jun,Zhang, Xinzhi,Zhang, Yangyang,Zhao, Jincheng

supporting information, p. 5772 - 5776 (2021/07/12)

A highly efficient base-, metal-, and ox...

B(C6F5)3-Catalyzed site-selective N1-alkylation of benzotriazoles with diazoalkanes

Guo, Jing,Mandal, Dipendu,Stephan, Douglas W.,Wu, Yile,Zhao, Yunbo

supporting information, p. 7758 - 7761 (2021/08/13)

Alkylation of benzotriazoles is syntheti...

23786-14-3 Process route

methanol
67-56-1

methanol

diethyl (2-(4-methoxyphenyl)-2-oxoethyl) phosphate
113680-16-3

diethyl (2-(4-methoxyphenyl)-2-oxoethyl) phosphate

4-methoxy-phenyl acetic acid methyl ester
23786-14-3

4-methoxy-phenyl acetic acid methyl ester

1-(4-methoxyphenyl)ethanone
100-06-1

1-(4-methoxyphenyl)ethanone

Conditions
Conditions Yield
at 40 ℃; Quantum yield; Irradiation;
UV-irradiation;
methanol
67-56-1

methanol

2-chloro-1-(4-methoxyphenyl)ethanone
2196-99-8

2-chloro-1-(4-methoxyphenyl)ethanone

4-chloromethoxybenzene
623-12-1

4-chloromethoxybenzene

4-methoxy-phenyl acetic acid methyl ester
23786-14-3

4-methoxy-phenyl acetic acid methyl ester

1-(4-methoxyphenyl)ethanone
100-06-1

1-(4-methoxyphenyl)ethanone

Conditions
Conditions Yield
With methyloxirane; for 4h; Mechanism; Product distribution; Irradiation; other α-chloro acetophenones, various solvents, other reaction time;
35%
34%
17%
With methyloxirane; for 4h; Irradiation;
35%
17%
34%

23786-14-3 Upstream products

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    6832-17-3

    2-diazo-1-(4-methoxyphenyl)ethanone

  • 532-31-0
    532-31-0

    silver benzoate

  • 156-38-7
    156-38-7

    4-hydroxyphenylacetate

  • 74-88-4
    74-88-4

    methyl iodide

23786-14-3 Downstream products

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    14028-72-9

    (4-methoxy-phenyl)-acetic acid-(4-benzyloxy-3-methoxy-phenethylamide)

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    56369-49-4

    (4-methoxy-phenyl)-acetic acid-(2-hydroxy-ethylamide)

  • 53673-37-3
    53673-37-3

    N-(2-amino-ethyl)-2-(4-methoxy-phenyl)-acetamide

  • 63732-96-7
    63732-96-7

    17-(4-methoxy-phenethyl)-morphinan-3-ol

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