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3-Oxa-10-azacyclobut[3,4]indeno[5,6-a]fluorene,1,2,2a,10,10c,11,11a,11b-octahydro-2a,4,11,11-tetramethyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31077-94-8

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31077-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31077-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,7 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31077-94:
(7*3)+(6*1)+(5*0)+(4*7)+(3*7)+(2*9)+(1*4)=98
98 % 10 = 8
So 31077-94-8 is a valid CAS Registry Number.

31077-94-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclomahanimbine

1.2 Other means of identification

Product number -
Other names Bicyclomahamimbin

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:31077-94-8 SDS

31077-94-8Upstream product

31077-94-8Downstream Products

31077-94-8Relevant academic research and scientific papers

A simple BF3?Et2O-mediated cycloaddition reaction to the formation of cyclic monoterpenoid pyrano[3,2-a]carbazole alkaloids

Tan, Siow-Ping,Nafiah, Mohd Azlan

, p. 395 - 399 (2021/09/07)

A Lewis acid BF3?Et2O-mediated intramolecular cycloaddition reaction of mahanimbine (1) is described. Three cycloadducts, bicyclomahanimbine (2), cyclomahanimbine (3) and murrayazolinine (4) were obtained. The structural characterization of these compounds was determined by 1D and 2D NMR experiments. These compounds showed no cytotoxic activity against human MRC-5 cells (IC50 > 60 μg/mL). Compound 3 showed the highest inhibition cytotoxic effects against HeLa and HL-60 cancer cells with IC50 values of 10.0 and 28.7 μg/mL, respectively. This strategy opens a new approach for the synthesis of biologically significant cyclic monoterpenoid pyrano[3,2-a]carbazole alkaloids.

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