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Benzene, 1-[[[(3E)-4-iodo-3-pentenyl]oxy]methyl]-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

500702-36-3

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500702-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 500702-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,0 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 500702-36:
(8*5)+(7*0)+(6*0)+(5*7)+(4*0)+(3*2)+(2*3)+(1*6)=93
93 % 10 = 3
So 500702-36-3 is a valid CAS Registry Number.

500702-36-3SDS

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 1-(4-iodopent-3-enoxymethyl)-4-methoxybenzene

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:500702-36-3 SDS

500702-36-3Relevant academic research and scientific papers

Versatile enantiocontrolled synthesis of (+)-fostriecin.

Esumi, Tomoyuki,Okamoto, Nanako,Hatakeyama, Susumi

, p. 3042 - 3043 (2002)

Fostriecin, a potent protein phosphatase inhibitor and antitumor agent, has been enantioselectively synthesized in naturally occurring form via a versatile route, which also allows one to secure all possible stereoisomeres of the C1-C13 fragment including

Total synthesis of (+)-fostriecin and (+)-phoslactomycin B

Shibahara, Setsuya,Fujino, Masataka,Tashiro, Yasumasa,Okamoto, Nanako,Esumi, Tomoyuki,Takahashi, Keisuske,Ishihara, Jun,Hatakeyama, Susumi

experimental part, p. 2935 - 2953 (2010/03/03)

(+)-Fostriecin and (+)-phoslactomycin B, which are potent and selective inhibitors of protein phosphatase, were synthesized by a highly enantio-and stereoselective approach that enabled us to prepare all possible isomers at both the C11 secondary alcohol position and the δ12-double bond. Georg Thieme Verlag Stuttgart.

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