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7785-64-0

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7785-64-0 Usage

Description

Butyl 2-methylcrotonate, also known as 2-methyl-2-butyl crotonate, is a chemical compound that is widely 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 typically derived from crotonic acid and butanol and is commonly found in a variety of products such as perfumes, cosmetics, soaps, and air fresheners.

Uses

Used in Flavor and Fragrance Industry:
Butyl 2-methylcrotonate is used as a flavoring and fragrance ingredient for its desirable fruity, green, and slightly floral odor. It is commonly used in perfumes, cosmetics, soaps, and air fresheners to provide a pleasant and attractive scent.
Used in Food Industry:
Butyl 2-methylcrotonate is used as a flavoring agent in the food industry for various fruit and floral flavors. It enhances the taste and aroma of food products, making them more appealing to consumers.
Used in Pharmaceutical Industry:
Butyl 2-methylcrotonate is used in the production of pharmaceuticals due to its desirable odor and properties. It can be used as a solvent or carrier for active pharmaceutical ingredients, improving the efficacy and acceptability of medications.
Used in Lubricant and Plasticizer Production:
Butyl 2-methylcrotonate is also used in the production of lubricants and plasticizers due to its desirable properties. It can improve the performance and longevity of these products, making them more effective and useful in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7785-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7785-64:
(6*7)+(5*7)+(4*8)+(3*5)+(2*6)+(1*4)=140
140 % 10 = 0
So 7785-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c1-4-6-7-11-9(10)8(3)5-2/h5H,4,6-7H2,1-3H3/b8-5-

7785-64-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl (Z)-2-methylbut-2-enoate

1.2 Other means of identification

Product number -
Other names Butyl (2Z)-2-methyl-2-butenoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7785-64-0 SDS

7785-64-0Relevant articles and documents

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 dwarf aromatic shrub native to the Mediterranean region. The typical subspecies (italicum) produces an essential oil rich in neryl acetate and characteristic β-diketones, italidiones, highly valued in the perfume industry. As esters are an important group of aroma-active volatiles, herein the composition of the ester fraction of this immortelle chemotype essential oil was studied in detail. Chromatographic separation of Corsican immortelle essential oil enabled the discovery of numerous potentially olfactory-interesting esters of nerol and/or angelic acid, undetectable by direct GC-MS analyses of the unfractioned oil. Four esters of nerol and medium-chain branched fatty acids represent new natural products, while several other esters have a rather restricted occurrence in the Plant Kingdom.

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

supporting information; experimental part, p. 1208 - 1212 (2012/07/28)

Undirected/Directed Cross-Coupling: A new dehydrogenative Rh III-catalyzed cross-coupling reaction between bromoarenes bearing no directing group and vinylic substrates substituted by a chelating group is reported. An original reaction mechanism enables the use of internal alkenes in a Z-selective coupling. The application of 1,3-disubstituted or 1,2-homodisubstituted arenes leads to the formation of highly functionalized, complex, and valuable olefins as one single isomer. Copyright

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