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Decahydro-4-isothiocyanato-1,1,4,7-tetramethyl-1H-cycloprop[e]azulene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56012-90-9

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56012-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56012-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,1 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56012-90:
(7*5)+(6*6)+(5*0)+(4*1)+(3*2)+(2*9)+(1*0)=99
99 % 10 = 9
So 56012-90-9 is a valid CAS Registry Number.

56012-90-9SDS

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 (-)-10(R)-Isothiocyanoaromadendrane

1.2 Other means of identification

Product number -
Other names axisothiocyanate-2

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:56012-90-9 SDS

56012-90-9Downstream Products

56012-90-9Relevant academic research and scientific papers

A direct route to terpene isothiocyanates

Da Silva,Almagro,Marsaioli

, p. 6717 - 6720 (1993)

An expedient entry into the preparation of isothiocyanate terpenes is presented. The method involves the addition of isothiocyanic acid prepared "in situ" to terminal double bonds.

Halichonadin F and the Cu(I) complex of halichonadin C from the sponge Halichondria sp.

Ishiyama, Haruaki,Kozawa, Shingo,Aoyama, Kazuki,Mikami, Yuzuru,Fromont, Jane,Kobayashi, Jun'ichi

, p. 1301 - 1303 (2008)

A new sesquiterpenoid with an aromadendrane skeleton, halichonadin F (1), and the Cu(I) complex of haliconadin C (2) were isolated from a marine sponge Halichondria sp., and the structures and relative stereochemistries of 1 and the complex of 2 were elucidated on the basis of spectroscopic data and chemical methods.

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