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53341-66-5

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53341-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53341-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,4 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53341-66:
(7*5)+(6*3)+(5*3)+(4*4)+(3*1)+(2*6)+(1*6)=105
105 % 10 = 5
So 53341-66-5 is a valid CAS Registry Number.

53341-66-5SDS

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 ethyl 3-anilino-3-oxopropanoate

1.2 Other means of identification

Product number -
Other names malonic acid monoethyl ester N-phenylcarboxamide

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:53341-66-5 SDS

53341-66-5Relevant articles and documents

THIENOPYRIDINE DERIVATIVES AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

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Paragraph 0228; 0229-0232, (2019/10/29)

Since a thienopyridine derivative compound represented by chemical formula 1 or a pharmaceutically acceptable salt thereof of the present invention has an excellent effect of inhibiting protein kinase activity, a pharmaceutical composition comprising the same can be usefully used for preventing or treating diseases related to protein kinase activity.COPYRIGHT KIPO 2020

AlCl 3 -Mediated Synthesis of 4-Aryl-2-quinolone-3-carboxylates

Yang, Seung-Hye,Jo, Seohyun,Shin, Dongyun

, p. 1614 - 1619 (2017/08/11)

4-Aryl-2-quinolones are important skeletons from both chemical and medicinal viewpoints. We herein report the development of an efficient synthetic method for 3-substituted 4-aryl-2-quinolones. The key reaction in this process involves an AlCl 3/sub

QUINOLINE DERIVATIVE

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Paragraph 0165; 0191, (2017/11/17)

This compound represented by general formula (I) and having a quinoline skeleton has a strong Axl inhibitory activity. Consequently, this compound can be a therapeutic agent for Axl-related diseases, for example, cancers such as acute myeloid leukemia, chronic myeloid leukemia, melanoma, breast cancer, pancreatic cancer and glioma, kidney diseases, immune system diseases and cardiovascular diseases.

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