Anisyl Formate

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pd_proNo:464389-dbe62610-d4f4-43a0-a185-2aee1d2b522c

pd_productuse:

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Detailed introduction

Anisyl Formate 122-91-8 with purity >99% Low price in stock

  • Molecular Formula:C9H10 O3
  • Molecular Weight:166.177
  • Vapor Pressure:6.159Pa at 25℃ 
  • Refractive Index:n20/D 1.523(lit.)  
  • Boiling Point:254.8°Cat760mmHg 
  • Flash Point:100.6°C 
  • PSA:35.53000 
  • Density:1.108g/cm3 
  • LogP:2.00410 

4-METHOXYBENZYL FORMATE(Cas 122-91-8) Usage

Preparation

By direct esterification of anisic alcohol with formic acid.

Flammability and Explosibility

Notclassified

Metabolism

Esters of benzyl alcohol, such as the acetate, are rapidly hydrolysed in vivo to benzyl alcohol, which is then oxidized. The expected general reaction of primary aromatic alcohols in the animal body is oxidation to the corresponding aromatic acid, which is usually excreted as a glycine conjugate and to a lesser extent as an ester glucuronide. In rabbits, benzyl alcohol is almost entirely converted to benzoic acid, which is excreted mainly as hippuric acid . In substituted anisoles with a carboxyl group or a potential carboxyl group attached to the aromatic ring, the ether link is relatively stable(Williams, 1959).

Aroma threshold values

Odor characteristics are sweet, spicy, vanilla-like with powdery fruity nuances.

Taste threshold values

Taste characteristics at 50 ppm: sweet, vanilla, spice, with fruity heliotropine-like nuances.

InChI:InChI=1/C9H10O3/c1-11-9-4-2-8(3-5-9)6-12-7-10/h2-5,7H,6H2,1H3

122-91-8 Relevant articles

Selective Production of Diethyl Maleate via Oxidative Cleavage of Lignin Aromatic Unit

Cai, Zhenping,Long, Jinxing,Li, Yingwen,Ye, Lin,Yin, Biaolin,France, Liam John,Dong, Juncai,Zheng, Lirong,He, Hongyan,Liu, Sijie,Tsang, Shik Chi Edman,Li, Xuehui

supporting information, p. 2365 - 2377 (2019/09/10)

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Method for preparing formate-type compound

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Paragraph 0039; 0047; 0048, (2018/07/30)

The invention discloses a method for pre...

Application of polydopamine sulfamic acid-functionalized magnetic Fe3O4 nanoparticles (Fe3O4@PDA-SO3H) as a heterogeneous and recyclable nanocatalyst for the formylation of alcohols and amines under solvent-free conditions

Taheri, Sepideh,Veisi, Hojat,Hekmati, Malak

, p. 5075 - 5081 (2017/07/11)

Herein, formylation of structurally diff...

Acidic ionic liquid immobilized on nanoporous Na+-montmorillonite as an efficient and reusable catalyst for the formylation of amines and alcohols

Shirini, Farhad,Mazloumi, Masoumeh,Seddighi, Mohadeseh

, p. 1759 - 1776 (2016/03/16)

In this work, nanoporous sodium montmori...

122-91-8 Process route

1,4-di(4-methoxyphenyl)ethanone
120-44-5

1,4-di(4-methoxyphenyl)ethanone

ethanol
64-17-5

ethanol

p-methylanizole
104-93-8

p-methylanizole

ethyl 4-methoxybenzoate
94-30-4

ethyl 4-methoxybenzoate

4-methoxy-, benzenemethanol, formate
122-91-8

4-methoxy-, benzenemethanol, formate

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

p-ethylanisole
1515-95-3

p-ethylanisole

Diethyl maleate
141-05-9

Diethyl maleate

succinic acid diethyl ester
123-25-1

succinic acid diethyl ester

Conditions
Conditions Yield
With [methyl-3-(butyl-4-sulfonate) imidazolium]CuPW12O40; oxygen; at 159.84 ℃; for 5h; under 6000.6 Torr;
4-Methoxybenzyl alcohol
105-13-5

4-Methoxybenzyl alcohol

formic acid ethyl ester
109-94-4

formic acid ethyl ester

4-methoxy-, benzenemethanol, formate
122-91-8

4-methoxy-, benzenemethanol, formate

Conditions
Conditions Yield
With K5; for 0.333333h; Heating;
98%
With Silphos; at 20 ℃; for 0.0833333h;
98%
(NH4)8[CeW10O36]*20H2O; for 3h; Heating;
95%
With silica-bonded N-propyl sulfamic acid; at 20 ℃; for 0.5h; chemoselective reaction;
94%
With sulfonic acid supported on polydopamine (PDA)-encapsulated Fe3O4 nanoparticles; In neat (no solvent); at 40 ℃; for 1h; Green chemistry;
90%

122-91-8 Upstream products

  • 77287-34-4
    77287-34-4

    formamide

  • 105-13-5
    105-13-5

    4-Methoxybenzyl alcohol

  • 64-18-6
    64-18-6

    formic acid

  • 195392-61-1
    195392-61-1

    4-formyloxy-1-[1'-(4-methoxybenzyloxy)propan-3'-yl]azetidin-2-one

122-91-8 Downstream products

  • 133788-00-8
    133788-00-8

    6-phenyl-3a,4-dihydro-1H-cyclopenta[c]furan-5(3H)-one

  • 67-56-1
    67-56-1

    methanol

  • 5405-95-8
    5405-95-8

    4,4'-dimethoxydibenzyl ether

  • 105-13-5
    105-13-5

    4-Methoxybenzyl alcohol

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