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ethyl 4-{[(2-chloroethyl)carbamoyl]amino}benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13908-47-9

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13908-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13908-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,0 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13908-47:
(7*1)+(6*3)+(5*9)+(4*0)+(3*8)+(2*4)+(1*7)=109
109 % 10 = 9
So 13908-47-9 is a valid CAS Registry Number.

13908-47-9SDS

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 ethyl 4-(2-chloroethylcarbamoylamino)benzoate

1.2 Other means of identification

Product number -
Other names ethyl 4-{[(2-chloroethyl)carbamoyl]amino}benzoate

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:13908-47-9 SDS

13908-47-9Downstream Products

13908-47-9Relevant academic research and scientific papers

SMALL MOLECULE ACTIVATORS OF NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) AND USES THEREOF

-

Paragraph 00676, (2018/08/03)

Provided herein are small molecule activators of Nicotinamide Phosphoribosyltransferase (NAMPT), compositions comprising the compounds, and methods of using the compounds and compositions.

Design, synthesis and evaluation of novel HDAC inhibitors as potential antitumor agents

Cheng, Jianjun,Qin, Jihong,Guo, Sihua,Qiu, Hangdeng,Zhong, Yun

, p. 4768 - 4772 (2015/01/09)

Phenyl imidazolidin-2-one was introduced as the linker for novel HDAC inhibitors. A focused library of 20 compounds was designed and synthesized, among which eight compounds showed equivalent or higher potencies against HDAC1 as compared to vorinostat. In vitro antitumor activity assays in HCT-116, PC-3 and HL-60 cancer cells revealed six compounds with potent antitumor activities, and compound 1o showed 6- to 9-fold higher potencies compared to vorinostat. In an HCT-116 nude mice xenograft model, compound 1o displayed significant antitumor activity in both continuous and intermittent dosing schedules.

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