Methyl 3,5-dimethoxybenzoate

  • Name: Methyl 3,5-dimethoxybenzoate
  • CAS: 2150-37-0
  • Purity: 99%
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Details

Top quality factory supply 2150-37-0 Methyl 3,5-dimethoxybenzoate at low price

  • Molecular Formula: C10H12O4
  • Molecular Weight: 196.203
  • Appearance/Colour: White to beige powder or granules 
  • Vapor Pressure: 0.00157mmHg at 25°C 
  • Melting Point: 41-43 °C 
  • Refractive Index: 1.497 
  • Boiling Point: 294.9 °C at 760 mmHg 
  • Flash Point: 128 °C 
  • PSA： 44.76000 
  • Density: 1.119 g/cm3 
  • LogP: 1.49040 

Methyl 3,5-dimethoxybenzoate(Cas 2150-37-0) Usage

General Description

Bromination of methyl 3,5-dimethoxybenzoate has been investigated.

InChI:InChI=1/C10H12O4/c1-12-8-4-7(10(11)14-3)5-9(6-8)13-2/h4-6H,1-3H3

2150-37-0 Relevant articles

Molecular modeling studies and: In vitro screening of dihydrorugosaflavonoid and its derivatives against Mycobacterium tuberculosis

Puranik, Ninad V.,Srivastava, Pratibha,Swami, Sagar,Choudhari, Amit,Sarkar, Dhiman

, p. 10634 - 10643 (2018)

Novel drug regimens against tuberculosis...

Synthesis of cannabinol by a modified Ullmann-ziegler cross-coupling

Nüllen, Max P.,G?ttlich, Richard

, p. 1109 - 1112 (2013)

Cannabinol, a pharmaceutically interesti...

Investigations on the Photochemical Reaction Mechanisms of Selected Dibenzoylmethane Compounds

Wang, Junxiao,Guo, Yan,Wang, Jialin,Ma, Jiani

supporting information, p. 7594 - 7602 (2021/06/21)

In this work, combined time-resolved spe...

Polyhydroxybenzoic acid derivatives as potential new antimalarial agents

Degotte, Gilles,Francotte, Pierre,Pirotte, Bernard,Frédérich, Michel

, (2021/08/07)

With more than 200 million cases and 400...

ANTIVIRAL COMPOUNDS AND THEIR USE

-

Paragraph 0081, (2021/04/10)

The invention relates to compounds that ...

Synthesis of [6,6,m]-Tricyclic Compounds via [4+2] Cycloaddition with Au or Cu Catalyst

Kang, Juyeon,Ham, Seunghwan,Seong, Chaehyeon,Oh, Chang Ho

supporting information, p. 1039 - 1043 (2021/05/05)

We synthesized [6,6,6]- and [6,6,7]-tric...

2150-37-0 Process route

4,6-dimethoxy-2-pyrone
21249-83-2

4,6-dimethoxy-2-pyrone

propynoic acid methyl ester
922-67-8

propynoic acid methyl ester

methyl 2, 4-dimethoxybenzoate
2150-41-6

methyl 2, 4-dimethoxybenzoate

methyl 3,5-dimethoxybenzoate
2150-37-0

methyl 3,5-dimethoxybenzoate

Conditions
Conditions Yield
at 200 ℃; for 2h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
3,4-Dihydroxybenzoic acid
99-50-3

3,4-Dihydroxybenzoic acid

4-hydroxysalicylic acid
89-86-1

4-hydroxysalicylic acid

3,4,5-trihydroxybenzoic acid
149-91-7

3,4,5-trihydroxybenzoic acid

3,5-Dihydroxybenzoic acid
99-10-5

3,5-Dihydroxybenzoic acid

2,3-Dihydroxybenzoic acid
303-38-8

2,3-Dihydroxybenzoic acid

2,5-dihydroxybenzoic acid.
490-79-9

2,5-dihydroxybenzoic acid.

3-Carboxyphenol
99-06-9

3-Carboxyphenol

salicylic acid
69-72-7,25496-36-0,8052-31-1

salicylic acid

methyl iodide
74-88-4

methyl iodide

4-hydroxy-benzoic acid
99-96-7

4-hydroxy-benzoic acid

methyl 2, 4-dimethoxybenzoate
2150-41-6

methyl 2, 4-dimethoxybenzoate

2-methoxybenzoic acid methyl ester
606-45-1

2-methoxybenzoic acid methyl ester

methyl 3-methoxybenzoate
5368-81-0

methyl 3-methoxybenzoate

methyl 4-methoxybenzoate
121-98-2

methyl 4-methoxybenzoate

methyl 3,4-dimethoxybenzoate
2150-38-1

methyl 3,4-dimethoxybenzoate

3,4,5-trimethoxybenzoic acid methyl ester
1916-07-0

3,4,5-trimethoxybenzoic acid methyl ester

methyl 2,3-dimethoxybenzoate
2150-42-7

methyl 2,3-dimethoxybenzoate

methyl 2,5-dimethoxybenzoate
2150-40-5

methyl 2,5-dimethoxybenzoate

methyl 3,5-dimethoxybenzoate
2150-37-0

methyl 3,5-dimethoxybenzoate

Conditions
Conditions Yield
3,4-Dihydroxybenzoic acid; 4-hydroxysalicylic acid; 3,4,5-trihydroxybenzoic acid; 3,5-Dihydroxybenzoic acid; 2,3-Dihydroxybenzoic acid; 2,5-dihydroxybenzoic acid.; 3-Carboxyphenol; salicylic acid; 4-hydroxy-benzoic acid; With sodium hydride; In hexane; N,N-dimethyl-formamide; at 25 ℃; for 2h; Inert atmosphere; Cooling with ice;
methyl iodide; In hexane; N,N-dimethyl-formamide; for 72h; Inert atmosphere;

2150-37-0 Upstream products

  • 186581-53-3
    186581-53-3

    diazomethane

  • 1132-21-4
    1132-21-4

    3,5-dimethoxybenzoic acid

  • 67-56-1
    67-56-1

    methanol

  • 99-10-5
    99-10-5

    3,5-Dihydroxybenzoic acid

2150-37-0 Downstream products

  • 41497-28-3
    41497-28-3

    3,5-Dimethoxy-α-(methylsulfonyl)acetophenon

  • 141524-36-9
    141524-36-9

    methyl 1-(4-bromobutyl)-3,5-dimethoxylcyclohexa-2,5-diene-1-carboxylate

  • 141524-40-5
    141524-40-5

    methyl 1-(4-chlorobutyl)-3,5-dimethoxycyclohexa-2,5-diene-1-carboxylate

  • 141524-37-0
    141524-37-0

    methyl 1-(5-bromopentyl)-3,5-dimethoxylcyclohexa-2,5-diene-1-carboxylate

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