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71357-60-3

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71357-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71357-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,3,5 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71357-60:
(7*7)+(6*1)+(5*3)+(4*5)+(3*7)+(2*6)+(1*0)=123
123 % 10 = 3
So 71357-60-3 is a valid CAS Registry Number.

71357-60-3SDS

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 racemic epijoubertinamine

1.2 Other means of identification

Product number -
Other names (+/-)-joubertinamine

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:71357-60-3 SDS

71357-60-3Relevant articles and documents

Total synthesis of (±)-joubertinamine from 3-(3,4-dimethoxyphenyl)- 5-bromo-2-pyrone

Tam, Nguyen Thanh,Cho, Cheon-Gyu

, p. 3391 - 3392 (2008/02/12)

The regioselective synthesis and Diels-Alder cycloaddition of 3-(3,4-dimethoxyphenyl)-5-bromo-2-pyrone provided a new efficient synthetic route to joubertinamine (9.6% total yield over 10 steps).

A Synthesis of Seco-mesembrane Alkaloids, (+/-)-Joubertiamine, (+/-)-Joubertinamine, and (+/-)-Epijoubertinamine

Hoshino, Osamu,Ishizaki, Miyuki,Sawaki, Shohei,Yuasa, Masayuki,Umezawa, Bunsuke

, p. 3373 - 3380 (2007/10/02)

A synthesis of seco-mesembrane alkaloids, (+/-)-joubertiamine (4), (+/-)-joubertinamine (5), and (+/-)-epijoubertinamine (6), was accomplished starting with 2-allyl-2-aryl-5,5-ethylenedioxycyclohexanones (10 and 3), which are readily available by allylati

SCELETIUM (AIZOACEAE) ALKALOIDS: TOTAL SYNTHESIS OF RACEMIC MESEMBRANONE, JOUBERTINAMINE AND EPIJOUBERTINAMINE

Sanchez, Ignacio H.,Soria, Jose de Jesus,Larraza, Maria Isabel,Flores, Humberto J.

, p. 551 - 554 (2007/10/02)

The total synthesis of the Sceletium alkaloids mesembranone, joubertinamine and epijoubertinamine via the intramolecular cyclization of an enone to a benzensulfonamide grouping under the conditions of a dissolving metal reduction is described.

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