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66949-73-3

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66949-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66949-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,4 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66949-73:
(7*6)+(6*6)+(5*9)+(4*4)+(3*9)+(2*7)+(1*3)=183
183 % 10 = 3
So 66949-73-3 is a valid CAS Registry Number.

66949-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-salicylidene-glycine ethyl ester

1.2 Other means of identification

Product number -
Other names N-(2-Hydroxy-benzyliden)-glycin-ethylester

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:66949-73-3 SDS

66949-73-3Relevant articles and documents

Platinum(II) complexes of reduced amino acid ester Schiff bases: Synthesis, characterization, and antitumor activity

Li, Li-Jun,Wang, Cheng,Qiao, Yu,Yang, Xiao-Yan,Hua, Xing-Xing,Du, Jian-Long

, p. 413 - 424 (2014)

A series of platinum(II) complexes of reduced amino acid esters Schiff bases were synthesized as potential anticancer agents and characterized by 1H NMR, EA, IR, and molar conductivity. These compounds were tested for their DNA interaction with salmon sperm DNA by ultraviolet spectrum and CD spectrum, and their in vitro anticancer activities have been validated against HL-60, KB, BGC-823, and Bel-7402 cell lines by MTT assay. The cytotoxicity of complexes 5d and 5f are better than cisplatin against Bel-7402 cell lines, and show a close cytotoxic effect against HL-60 cell line.

Synthesis of substituted 3-aminocoumarins from ethyl N-2- hydroxyarylideneglycinates

Khoo, Lian Ee

, p. 2533 - 2537 (2007/10/03)

3-Aminocoumarin and its derivatives are prepared by a thermal (150- 170°C) conversion reaction on the corresponding ethyl N-2- hydroxyarylideneglycinates,[2-HOC6H3(X)CH=NCH2CO2C2Hs; X = H, 5-Br, 5- OH, 5-NO2, 3-OMe, 4-OMe, and 5,6-benzo], which are synthesized by condensing ethyl glycinate hydrochloride with substituted salicylaldehyde.

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