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36518-04-4

36518-04-4

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36518-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36518-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,5,1 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36518-04:
(7*3)+(6*6)+(5*5)+(4*1)+(3*8)+(2*0)+(1*4)=114
114 % 10 = 4
So 36518-04-4 is a valid CAS Registry Number.

36518-04-4SDS

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 Athanasin

1.2 Other means of identification

Product number -
Other names (2S,5R)-5-Methyl-5-(4-methyl-furan-2-ylmethyl)-2,3,4,5-tetrahydro-[2,3']bifuranyl

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:36518-04-4 SDS

36518-04-4Downstream Products

36518-04-4Relevant articles and documents

FIRST SYNTHESIS OF THE DIFURANSESQUITERPENE ATHANASIN AND THE ELUCIDATION OF ITS RELATIVE AND ABSOLUTE CONFIGURATION

Bojack, Guido,Bornowski, Hans

, p. 9179 - 9186 (2007/10/02)

The synthesis of the naturally occurring difuransesquiterpene athanasin is described.Employing Seebach's method of "self-reproduction of chirality", the chiral oxirane 6 is built up, which is successively connected with suitable furan building blocks.Cyclization of the resulting diols 14a/b gives the enantiomerically pure diastereomers 1a and 1b.Comparison of their spectroscopic data with athanasin after separation allows the elucidation of the natural product's relative and absolute configuration. Key Words: Difuransesquiterpene; natural product synthesis; special furan building blocks; relative and absolute configuration; optical rotations

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