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52762-28-4

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52762-28-4 Usage

Molecular structure

The compound has a complex and long molecular structure with multiple rings and functional groups.

Functional groups

The presence of hydroxy, methoxy, and carbamate groups in the molecule contributes to its chemical properties and reactivity.

Potential applications

Due to its unique structure and functional groups, the compound may have potential applications in medicinal chemistry, pharmacology, or material science.

Further research needed

The properties and potential uses of this compound are not yet fully characterized, and additional research is required to determine its full potential.

Check Digit Verification of cas no

The CAS Registry Mumber 52762-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,6 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52762-28:
(7*5)+(6*2)+(5*7)+(4*6)+(3*2)+(2*2)+(1*8)=124
124 % 10 = 4
So 52762-28-4 is a valid CAS Registry Number.

52762-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(8E,12Z,14E)-6,22-dihydroxy-5,11-dimethoxy-3,7,9,15-tetramethyl-16,20,21-trioxo-17-azabicyclo[16.3.1]docosa-1(22),8,12,14,18-pentaen-10-yl] carbamate

1.2 Other means of identification

Product number -
Other names 17-Des-O-methylgeldanamycin

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:52762-28-4 SDS

52762-28-4Upstream product

52762-28-4Downstream Products

52762-28-4Relevant articles and documents

Synthesis and biological evaluation of a new class of geldanamycin derivatives as potent inhibitors of Hsp90

Le Brazidec, Jean-Yves,Kamal, Adeela,Busch, David,Thao, Lia,Zhang, Lin,Timony, Gregg,Grecko, Roy,Trent, Katy,Lough, Rachel,Salazar, Tim,Khan, Samina,Burrows, Francis,Boehm, Marcus F.

, p. 3865 - 3873 (2007/10/03)

The heat shock protein Hsp90 has increasingly become an important therapeutic target especially for treatment of cancers. Inhibition of the ATPase activity of Hsp90 by natural products (e.g., 17-allylaminogeldanamycin or radicicol) leads to the ubiquitina

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