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20007-82-3

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20007-82-3 Usage

General Description

Ipomeamarone is a naturally occurring chemical found in the Ipomoea plant, specifically in the seeds of Ipomoea carnea, which is commonly known as white morning glory. It belongs to a class of compounds known as naphthoquinones, and has been found to exhibit potential anticancer and cytotoxic properties. Studies have shown that ipomeamarone can induce cell death in various cancer cell lines, making it a potential candidate for the development of new anticancer drugs. However, further research is needed to fully understand its mechanism of action and its potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 20007-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,0 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20007-82:
(7*2)+(6*0)+(5*0)+(4*0)+(3*7)+(2*8)+(1*2)=53
53 % 10 = 3
So 20007-82-3 is a valid CAS Registry Number.

20007-82-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name BOHLMANN 176

1.2 Other means of identification

Product number -
Other names trans-4-methyl-1-(2,3,4,5-tetrahydro-5-methyl<2,3'-bifuran>-5-yl)-2-pentanone

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:20007-82-3 SDS

20007-82-3Downstream Products

20007-82-3Relevant articles and documents

Formal Total Synthesis of Ipomeamarone via the Dihydrofuran Annulation

Hudlicky, Tomas,Lovelace, Thomas C.

, p. 1721 - 1732 (2007/10/02)

A formal synthesis of (2R-cis)-4-methyl-1-(2,3,4,5-tetrahydro)-5-methyl--2-pentanone, or ipomeamarone (1) was accomplished from 3-furaldehyde 5 and ethyl-2-bromocrotonate 4.The key step involved the formation of the dihydrofuran ring in 2 via a vinyloxirane rearrangement of 3 in the dihydrofuran annulation.Mechanistic duality of reactions of those tetrahydrofurans possessing acidic hydrogens adjacent to the ring is addressed.

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