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1190-91-6

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1190-91-6 Usage

General Description

3-Buten-2-one, 4-(dimethylamino)- (6CI,7CI,8CI,9CI), also known as dimethylaminocrotonaldehyde, is a chemical compound with the molecular formula C7H11NO. It is an organic compound that belongs to the ketone and amine functional group. 3-Buten-2-one, 4-(dimethylamino)- (6CI,7CI,8CI,9CI) is a pale yellow liquid with a pungent odor and is soluble in water and most organic solvents. It is commonly used as a reagent in organic synthesis and as a precursor for various pharmaceuticals and agrochemicals. Additionally, it has applications as a flavoring agent in the food industry and as a fragrance in the cosmetic and personal care industry. However, it is important to handle this compound with caution as it is known to be a irritant to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 1190-91-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1190-91:
(6*1)+(5*1)+(4*9)+(3*0)+(2*9)+(1*1)=66
66 % 10 = 6
So 1190-91-6 is a valid CAS Registry Number.

1190-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl β-(dimethylamino)vinyl ketone

1.2 Other means of identification

Product number -
Other names (3E)-4-(Dimethylamino)-3-Buten-2-One

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:1190-91-6 SDS

1190-91-6Relevant articles and documents

Reactions of enaminoketones with CH-acidic compounds (author's transl)

Eiden,Herdeis

, p. 287 - 293 (1978)

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An expedient synthesis of highly functionalized 1,3-dienes by employing cyclopropenes asC4units

Jiang, Chengzhou,Wu, Jiamin,Han, Jiabin,Chen, Kai,Qian, Yang,Zhang, Zhengyu,Jiang, Yaojia

supporting information, p. 5710 - 5713 (2021/06/16)

An efficient method has been described to synthesize dicarbonyl functionalized 1,3-dienes by cleaving the CC bond of enaminones with cyclopropenes in the presence of a rhodium catalyst. The acetate-substituted cyclopropenes are judiciously chosen as standardC4units of 1,3-diene precursors. The reactions are believed to undergo a unique cutting and insertion process, involving a CC bond cleavage of the enaminone and insertion of a newC(sp2) source with the formation of two C-C single bonds. A broad range of substrates can be used to synthesize the corresponding 1,3-dienes under very mild reaction conditions, including low catalyst-loading, ambient temperature, and a neutral reaction solvent.

METHOD FOR PRODUCING NITROGEN-CONTAINING COMPOUND

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Paragraph 0086-0095, (2020/02/20)

Provided is an efficient and economical production method of a nitrogen-containing compound. A method for producing a compound represented by the formula R3C(O)CH═CHNR1R2, including reacting a compound represented by the following formula (4) with more than 6-fold moles of a compound represented by the formula NR1R2C(O)H to give a reaction mixture of the compound represented by the formula (4) and the compound represented by the formula NR1R2C(O)H, and reacting the reaction mixture with a compound represented by the formula R3C(O)CH3 by using a basic compound: wherein X is a halogen atom and R1, R2 and R3 are each independently an alkyl group having 1-6 carbon atoms.

Compound preparation method

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Paragraph 0017-0026, (2019/04/17)

The invention relates to a compound preparation method. Organic solvents and sodium methylate are added into a reaction vessel, carbon monoxide is led into the reaction vessel to perform reaction, acetone and organic solvent mixed solution is dropped after reaction to continue reaction to generate an intermediate sodium salt as shown in a formula I, the intermediate sodium salt reacts with dimethylamine to generate 4-N, N-dimethyl butene-3-ketone as shown in a formula II. Synthesis steps can be finished in one vessel, and the compound preparation method is low in cost and suitable for industrialization production.

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