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1H-Indole, 3-[2-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-5-oxazolyl]-1-(methoxy methyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

570377-01-4

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570377-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 570377-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,0,3,7 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 570377-01:
(8*5)+(7*7)+(6*0)+(5*3)+(4*7)+(3*7)+(2*0)+(1*1)=154
154 % 10 = 4
So 570377-01-4 is a valid CAS Registry Number.

570377-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-(tert-Butyl-diphenyl-silanyloxymethyl)-oxazol-5-yl]-1-methoxymethyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indole

1.2 Other means of identification

Product number -
Other names -

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:570377-01-4 SDS

570377-01-4Relevant academic research and scientific papers

Chemistry and biology of diazonamide A: Second total synthesis and biological investigations

Nicolaou,Hao, Junliang,Reddy, Mali V.,Rao, Paraselli Bheema,Rassias, Gerasimos,Snyder, Scott A.,Huang, Xianhai,Chen, David Y.-K.,Brenzovich, William E.,Giuseppone, Nicolas,Giannakakou, Paraskevi,O'Brate, Aurora

, p. 12897 - 12906 (2007/10/03)

As an especially unique target for chemical synthesis, diazonamide A has the potential to be constructed through a plethora of synthetic routes, each attended by different challenges and opportunities for discovery. In this article, we detail our second total synthesis of diazonamide A through a sequence entirely distinct from that employed in our first campaign, one whose success required the development of several special strategies and tactics. We also disclose our complete studies regarding the chemical biology of diazonamide A and its structural congeners, and more fully delineate the scope of our protocol for Robinson-Gabriel cyclodehydration using pyridine-buffered POCl 3.

The second total synthesis of diazonamide A

Nicolaou,Bheema Rao, Paraselli,Hao, Junliang,Reddy, Mali Venkat,Rassias, Gerasimos,Huang, Xianhai,Chen, David Y.-K.,Snyder, Scott A.

, p. 1753 - 1758 (2007/10/03)

The uniquely woven, highly strained molecular architecture and the potent antitumor activity of diazonamide A (1) make this natural product an attractive synthetic target. The key steps in this total synthesis of 1 include a novel Sml2-induced

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