Welcome to LookChem.com Sign In|Join Free
  • or
ethyl 4-hydroxy-6-nitro-naphthalene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79290-07-6

Post Buying Request

79290-07-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

79290-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79290-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,9 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79290-07:
(7*7)+(6*9)+(5*2)+(4*9)+(3*0)+(2*0)+(1*7)=156
156 % 10 = 6
So 79290-07-6 is a valid CAS Registry Number.

79290-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-hydroxy-6-nitro-2-naphthoate

1.2 Other means of identification

Product number -
Other names ethyl 4-hydroxy-6-nitro-2-naphthalenecarboxylate

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:79290-07-6 SDS

79290-07-6Relevant academic research and scientific papers

ASYMMETRIC CONJUGATE COMPOUNDS

-

Page/Page column 180-181, (2017/12/01)

The invention relates to compound of formula (I): A-X1-L-X2-B and salts, solvates and tautomers thereof, which are useful as medicaments, in particular as anti-proliferative agents and for use as a drug in an antibody-drug conjugate;

Design, synthesis and cytotoxicity evaluation of 1-chloromethyl-5-hydroxy-1,2-dihydro-3H-benz[e]indole (seco-CBI) dimers

Jia, Guofeng,Lown, J. William

, p. 1607 - 1617 (2007/10/03)

Three types of 1-chloromethyl-5-hydroxy-1,2-dihydro-3H-benz[e]indole (seco-CBI) dimers were designed, synthesized and evaluated in vitro by NCI against nine types of cancer cells. Biological results showed that the antitumor activities of these seco-CBI dimers were strongly related to the position and length of the linker and generally with potency increasing in the order of C7-C7 dimers (22i-iv)50 values50 values0.01μM against all the cell lines and showed the highest overall potency of the agents examined (GMG=0.0120μM). Copyright (C) 2000 Elsevier Science Ltd.

Substituted naphthoic acids

-

, (2008/06/13)

Certain ureides of substituted naphthoic acids and salts useful as inhibitors of connective tissue destruction.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 79290-07-6