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3413-59-0

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  • benzene-1,3-dicarboxylic acid; 2,2-dimethylpropane-1,3-diol; 2-ethyl-2-(hydroxymethyl)propane-1,3-diol; hexanedioic acid; propane-1,2-diol

    Cas No: 3413-59-0

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3413-59-0 Usage

General Description

(4-Butoxyphenyl)acetamide is a chemical compound with the molecular formula C12H17NO2. It is a derivative of acetamide and contains a butoxyphenyl group, which is a combination of a butoxy group and a phenyl group. (4-BUTOXYPHENYL)ACETAMIDE is commonly used in the manufacturing of pharmaceuticals and as an intermediate in organic synthesis. It has applications in the production of various drugs and pharmaceutical products. Additionally, it may also have potential uses in the field of medicine and research due to its chemical properties and structure. Overall, (4-Butoxyphenyl)acetamide is a versatile chemical compound with a range of potential applications in the pharmaceutical and medical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 3413-59-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,1 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3413-59:
(6*3)+(5*4)+(4*1)+(3*3)+(2*5)+(1*9)=70
70 % 10 = 0
So 3413-59-0 is a valid CAS Registry Number.

3413-59-0 Well-known Company Product Price

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  • Sigma-Aldrich

  • (Y0001732)  Bufexamac impurity D  EuropePharmacopoeia (EP) Reference Standard

  • 3413-59-0

  • Y0001732

  • 1,880.19CNY

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3413-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-butoxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names 2-(p-Butoxyphenyl)acetamide

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:3413-59-0 SDS

3413-59-0Downstream Products

3413-59-0Relevant articles and documents

Design of Inhibitors from the Three-Dimensional Structure of Alcohol Dehydrogenase. Chemical Synthesis and Enzymatic Properties

Freudenreich, Charles,Samama, Jean-Pierre,Biellmann, Jean-Francois

, p. 3344 - 3353 (2007/10/02)

Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.

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