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2H-Pyran-4-ol, 2-[2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl]tetrahydro-6-[(1E)-2-iodo- 1-methylethenyl]-3,5-dimethyl-, (2R,3R,4S,5R,6R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

867033-63-4

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867033-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 867033-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,7,0,3 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 867033-63:
(8*8)+(7*6)+(6*7)+(5*0)+(4*3)+(3*3)+(2*6)+(1*3)=184
184 % 10 = 4
So 867033-63-4 is a valid CAS Registry Number.

867033-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R,4S,5R,6R)-2-(2-((tert-butyldiphenylsilyl)oxy)ethyl)-6-((E)-1-iodoprop-1-en-2-yl)-3,5-dimethyltetrahydro-2H-pyran-4-ol

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:867033-63-4 SDS

867033-63-4Relevant academic research and scientific papers

Phorboxazole compounds and methods of their preparation

-

Page/Page column 46-47, (2009/02/11)

Novel macrolactone compounds, their methods of preparation, pharmaceutical compositions containing these compounds, and methods for their pharmaceutical use are disclosed. In certain embodiments, the macrolactone compounds may be useful, inter alia, for treating various cancers, inducing apoptosis in malignant cells, or inhibiting cancer cell division.

(+)-Phorboxazole a synthetic studies. A highly convergent, second generation total synthesis of (+)-phorboxazole A

Smith III, Amos B.,Razler, Thomas M.,Ciavarri, Jeffrey P.,Hirose, Tomoyasu,Ishikawa, Tomoyasu

, p. 4399 - 4402 (2007/10/03)

(Chemical Equation Presented) A second generation total synthesis of the potent antitumor agent (+)-phorboxazole A (1) has been achieved. The cornerstone of this approach comprises a more convergent strategy, involving late-stage Stille union of a fully e

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