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90316-38-4

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90316-38-4 Usage

General Description

"(2E)-3-(4-methoxyphenyl)-N,N-dimethylbut-2-enamide" is an organic chemical compound with a molecular formula C13H19NO2. It is a member of the amide class of compounds and is used in various applications, including pharmaceuticals and organic synthesis. (2E)-3-(4-methoxyphenyl)-N,N-dimethylbut-2-enamide has a but-2-enamide functional group and a 4-methoxyphenyl group, which gives it its characteristic properties. It is commonly used as an intermediate in the synthesis of other organic compounds and has potential applications in the pharmaceutical industry for the development of new drugs. Overall, "(2E)-3-(4-methoxyphenyl)-N,N-dimethylbut-2-enamide" is a versatile chemical with wide-ranging potential in various scientific and industrial fields.

Check Digit Verification of cas no

The CAS Registry Mumber 90316-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,1 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90316-38:
(7*9)+(6*0)+(5*3)+(4*1)+(3*6)+(2*3)+(1*8)=114
114 % 10 = 4
So 90316-38-4 is a valid CAS Registry Number.

90316-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(4-methoxyphenyl)-N,N-dimethylbut-2-enamide

1.2 Other means of identification

Product number -
Other names -

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:90316-38-4 SDS

90316-38-4Downstream Products

90316-38-4Relevant articles and documents

Nickel-catalyzed cross-coupling of β-carbonyl alkenyl pivalates with arylzinc chlorides

Pan, Wen-Jing,Wang, Zhong-Xia

, p. 1029 - 1036 (2018/02/19)

The nickel-catalyzed cross-coupling reaction of β-carbonyl alkenyl pivalates with arylzinc reagents generates 3-aryl-substituted α,β-unsaturated carbonyl compounds via C-O bond cleavage. The reaction features mild reaction conditions, a wide scope of substrates, and good functional group tolerance.

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