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18312-21-5

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18312-21-5 Usage

General Description

Trans-isomyristicin is a chemical compound found in nutmeg and other plants, and is classified as a phenylpropanoid. It is a stereoisomer of the more common myristicin compound, and is known for its psychoactive effects when consumed in large amounts. It has been reported to have hallucinogenic and deliriant properties, and is often used recreationally for its mind-altering effects. Additionally, trans-isomyristicin has been studied for its potential medicinal properties, including its anti-inflammatory and antioxidant effects. However, its use is also associated with potential toxic effects and should be used with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 18312-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,1 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18312-21:
(7*1)+(6*8)+(5*3)+(4*1)+(3*2)+(2*2)+(1*1)=85
85 % 10 = 5
So 18312-21-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O3/c1-3-4-8-5-9(12-2)11-10(6-8)13-7-14-11/h3-6H,7H2,1-2H3/b4-3+

18312-21-5SDS

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 4-methoxy-6-[(E)-prop-1-enyl]-1,3-benzodioxole

1.2 Other means of identification

Product number -
Other names EINECS 242-198-3

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:18312-21-5 SDS

18312-21-5Relevant articles and documents

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Shulgin

, p. 380,381 (1966)

-

The first diastereoselective synthesis of cinerins A-C, PAF-antagonistic macrophyllin-type bicyclo[3.2.1]octane neolignans, using a novel Pd-catalysed oxyarylation

Coy B., Ericsson D.,Cuca S., Luis E.,Sefkow, Michael

supporting information; experimental part, p. 2003 - 2005 (2010/07/03)

The first diastereoselective synthesis of PAF-antagonistic cinerins A-C, macrophyllin-type bicyclo[3.2.1]octane neolignans from Pleurothyrium cinereum, has been accomplished using a novel Pd-catalysed oxyarylation to afford a 2,3-dihydrobenzofuran as the key intermediate.

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