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Pentanamide, 2-amino-N-(4-methoxyphenyl)-4-methyl-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65540-65-0

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65540-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65540-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,4 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65540-65:
(7*6)+(6*5)+(5*5)+(4*4)+(3*0)+(2*6)+(1*5)=130
130 % 10 = 0
So 65540-65-0 is a valid CAS Registry Number.

65540-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-N-(4-methoxyphenyl)-4-methylpentanamide

1.2 Other means of identification

Product number -
Other names Pentanamide,2-amino-N-(4-methoxyphenyl)-4-methyl-,(S)

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:65540-65-0 SDS

65540-65-0Upstream product

65540-65-0Relevant academic research and scientific papers

Caproamide derivatives, its preparation method, intermediate and application

-

Paragraph 0098; 0099; 0100, (2017/03/24)

The invention discloses a caproamide derivative represented by formula A or a pharmaceutically acceptable salt thereof, wherein R1 is H or halogen; R2 is halogen, or C1-C4 alkyl, C1-C4 alkoxy, or a C3-C7 heterocyclic ring, the number of heteroatom in the heterocyclic ring is 1-3, and the heteroatom is nitrogen and/or oxygen; R0 is benzyl, substituted benzyl or C4 alkyl, and a substituent of substituted benzyl is C1-C3 alkyl. The invention also discloses a preparation method, an intermediate and an application of the caproamide derivative. The caproamide derivative provided by the invention has effective and better antibacterial function, and has higher application value in the medical field.

Synthesis of rupestonic acid amide derivatives and their in vitro activity against type A3 and B flu virus and herpes simplex I and II

Yong,Aisa

experimental part, p. 311 - 314 (2009/04/04)

Derivatives of rupestonic acid (5a-e) were synthesized and evaluated preliminarily at the National Center for Drug Screening (PRC) for antiviral activity against type A3 and B flu virus and HSV-I and HSV-II in order to improve the biological ac

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