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(12α,16α)-9,10-[Methylenebis(oxy)]galanthan is a complex organic compound with the molecular formula C37H62O4. It is a steroidal lactone, specifically a derivative of galanthamine, which is an alkaloid found in certain species of the Amaryllidaceae family. (12α,16α)-9,10-[Methylenebis(oxy)]galanthan is characterized by the presence of a methylenebis(oxy) bridge between carbons 9 and 10, and it exhibits a specific stereochemistry at the 12α and 16α positions. It is known for its potential neuroprotective properties and is being studied for its effects on cognitive function and neurodegenerative diseases. The compound's structure and biological activity make it a subject of interest in the field of medicinal chemistry and drug development.

6871-57-4

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6871-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6871-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,7 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6871-57:
(6*6)+(5*8)+(4*7)+(3*1)+(2*5)+(1*7)=124
124 % 10 = 4
So 6871-57-4 is a valid CAS Registry Number.

6871-57-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-α-lycorane

1.2 Other means of identification

Product number -
Other names 9,10-methylenedioxy-galanthane

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:6871-57-4 SDS

6871-57-4Downstream Products

6871-57-4Relevant academic research and scientific papers

Asymmetric Total Syntheses of (?)-α-Lycorane, (?)-Zephyranthine, and Formal Synthesis of (+)-Clivonine

Chen, Yong-Jian,Cai, Sen-Lin,Wang, Chuan-Chuan,Cheng, Jin-Duo,Kramer, S?ren,Sun, Xing-Wen

, p. 1309 - 1313 (2017/06/23)

An asymmetric route to (?)-α-lycorane and (?)-zephyranthine, and a formal total synthesis of (+)-clivonine were achieved. A pivotal intermediate, which serves as a potent precursor for the divergent syntheses of these natural products, was accessed by a diastereoselective Pd-catalyzed cinnamylation of an N-tert-butanesulfinyl imine.

Catalytic asymmetric hydrogenation of α-arylcyclohexanones and total synthesis of (-)-α-lycorane

Li, Gang,Xie, Jian-Hua,Hou, Jing,Zhu, Shou-Fei,Zhou, Qi-Lin

, p. 1597 - 1604 (2013/07/05)

An efficient catalytic asymmetric hydrogenation of racemic α-arylcyclohexanones with an ethylene ketal group at the 5-position of the cyclohexane ring via dynamic kinetic resolution has been developed, giving chiral α-arylcyclohexanols with two contiguous

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