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1-METHOXY-4-NITRO-2-(2-PROPYNYLOXY)BENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89228-66-0

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89228-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89228-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,2 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89228-66:
(7*8)+(6*9)+(5*2)+(4*2)+(3*8)+(2*6)+(1*6)=170
170 % 10 = 0
So 89228-66-0 is a valid CAS Registry Number.

89228-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-4-nitro-2-prop-2-ynoxybenzene

1.2 Other means of identification

Product number -
Other names 1-methoxy-4-nitro-2-(prop-2-yn-1-yloxy)benzene

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:89228-66-0 SDS

89228-66-0Downstream Products

89228-66-0Relevant academic research and scientific papers

TRIAZOLE COMPOUNDS THAT MODULATE HSP90 ACTIVITY

-

Page/Page column 214, (2008/06/13)

The present invention relates to substituted triazole compounds and compositions comprising substituted triazole compounds. The invention further relates to methods of inhibiting the activity of Hsp90 in a subject in need thereof and methods for preventing or treating hyperproliferative disorders, such as cancer, in a subject in need thereof comprising administering to the subject a substituted triazole compound of the invention, or a composition comprising such a compound.

Isomerization of 4-aminobenzofurans to 4-hydroxyindoles

Chilin,Rodighiero,Guiotto

, p. 309 - 312 (2007/10/03)

4-Amino-2-methylbenzofurans are quantitatively converted to 4-hydroxy- 2-methylindoles in acidic medium. The rearrangement mechanism involves the ring opening of the furan ring to produce an intermediate carbocation, which undergoes ring clo- sure to the

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