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N,N,6,9a-tetramethyl-12-(1-methylethyl)-1,3-dioxotetradecahydro-1H-3b,11-ethenophenanthro[1,2-c]furan-6-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53471-74-2

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53471-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53471-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,7 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53471-74:
(7*5)+(6*3)+(5*4)+(4*7)+(3*1)+(2*7)+(1*4)=122
122 % 10 = 2
So 53471-74-2 is a valid CAS Registry Number.

53471-74-2SDS

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 12-isopropyl-N,N,6,9a-tetramethyl-1,3-dioxo-3,3a,4,5,5a,6,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-3b,11-ethenophenanthro[1,2-c]furan-6-carboxamide

1.2 Other means of identification

Product number -
Other names -

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:53471-74-2 SDS

53471-74-2Upstream product

53471-74-2Downstream Products

53471-74-2Relevant academic research and scientific papers

New hepato protective agents. I. Maleopimaric acid 4α carboxamides

Danswan,Ramm,Taylor

, p. 2188 - 2189 (2007/10/09)

A number of amide derivatives of maleopimaric acid were synthesized and preliminary results on their protective activity against galactosamine induced liver damage in the rat are described. The compounds were found to display the highest level of protective activity producing significant lowering of serum GOT and GPT levels at a daily dose of 250-300 mg/kg. The LD50 of these compounds was typically in excess of 2000 mg/kg.

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