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butyl 2-methylcrotonate
  • Chemical Name: butyl 2-methylcrotonate
  • CAS No.: 7785-64-0

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  • Molecular Formula: C9H16 O2
  • Molecular Weight: 156.225
  • Vapor Pressure: 0.459mmHg at 25°C 
  • Boiling Point: 193.7°C at 760 mmHg 
  • Flash Point: 72.2°C 
  • PSA: 26.30000 
  • Density: 0.897g/cm3 
  • LogP: 2.29590 

butyl 2-methylcrotonate(Cas 7785-64-0) Usage

General Description

Butyl 2-methylcrotonate, also known as 2-methyl-2-butyl crotonate, is a chemical compound commonly used as a flavoring and fragrance ingredient. It is a clear, colorless liquid with a fruity, green, and slightly floral odor. This ester compound is usually derived from crotonic acid and butanol and is commonly found in a variety of products such as perfumes, cosmetics, soaps, and air fresheners. It is also used in the food industry as a flavoring agent for various fruit and floral flavors. Additionally, butyl 2-methylcrotonate is used in the production of pharmaceuticals, lubricants, and plasticizers due to its desirable odor and properties.

InChI:InChI=1/C9H16O2/c1-4-6-7-11-9(10)8(3)5-2/h5H,4,6-7H2,1-3H3/b8-5-

7785-64-0 Relevant articles

New neryl esters from Helichrysum italicum (Roth) G. Don (Asteraceae) essential oil

?or?evi?, Miljana R.,?ivkovi? Sto?i?, Milena Z.,Aksi?, Jelena M.,Gen?i?, Marija S.,Mladenovi?, Marko Z.,Radulovi?, Niko S.

supporting information, (2020/11/02)

Helichrysum italicum (immortelle) is a d...

Ligand-Controlled Palladium-Catalyzed Alkoxycarbonylation of Allenes: Regioselective Synthesis of α,β- and β,γ-Unsaturated Esters

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The palladium-catalyzed regioselective a...

Undirected arene and chelate-assisted olefin C-H bond activation: [Rh IIICp*]-catalyzed dehydrogenative alkene-arene coupling as a new pathway for the selective synthesis of highly substituted Z olefins

Wencel-Delord, Joanna,Nimphius, Corinna,Patureau, Frederic W.,Glorius, Frank

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Undirected/Directed Cross-Coupling: A ne...

ENZYMATIC ENANTIOSELECTIVE HYDROLYSIS OF 2,2-DIMETHYL-1,3-DIOXOLANE-4-CARBOXYLIC ESTERS

Pottie, M.,Eycken, J. Van der,Vandewalle, M.,Dewanckele, J. M.,Roeper, H.

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2,2-dimethyl-1,3-dioxolane-4-carboxylic ...

7785-64-0 Process route

2,3-dimethylbutene
590-19-2

2,3-dimethylbutene

carbon monoxide
201230-82-2

carbon monoxide

butan-1-ol
71-36-3

butan-1-ol

(E)-butyl 2-methylbut-2-enoate
7785-64-0,66917-60-0,7785-66-2

(E)-butyl 2-methylbut-2-enoate

Conditions
Conditions Yield
With 2-(diphenylphosphino)pyridine; palladium diacetate; trifluoroacetic acid; In toluene; at 110 ℃; for 20h; under 30003 Torr; regioselective reaction; Autoclave; Inert atmosphere;
43%
Tiglic acid
80-59-1

Tiglic acid

butan-1-ol
71-36-3

butan-1-ol

(E)-butyl 2-methylbut-2-enoate
7785-64-0,66917-60-0,7785-66-2

(E)-butyl 2-methylbut-2-enoate

Conditions
Conditions Yield
With sulfuric acid; Reflux; Inert atmosphere;
52%
With sulfuric acid; benzene; unter Entfernen des entstehenden Wassers;
With toluene-4-sulfonic acid; In benzene; Heating;

7785-64-0 Upstream products

  • 80-59-1
    80-59-1

    Tiglic acid

  • 71-36-3
    71-36-3

    butan-1-ol

  • 542-69-8
    542-69-8

    1-iodo-butane

  • 590-19-2
    590-19-2

    2,3-dimethylbutene

7785-64-0 Downstream products

  • 1380708-60-0
    1380708-60-0

    (Z)-butyl 3-(3-bromophenyl)-2-methylbut-2-enoate

  • 1380708-77-9
    1380708-77-9

    (Z)-butyl 3-(4-bromophenyl)-2-methylbut-2-enoate

  • 1380708-62-2
    1380708-62-2

    (Z)-butyl 3-(3-bromo-5-chlorophenyl)-2-methylbut-2-enoate

  • 1380708-61-1
    1380708-61-1

    (Z)-butyl 3-(3-bromo-5-(trifluoromethyl)phenyl)-2-methylbut-2-enoate