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5937-49-5

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5937-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5937-49-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5937-49:
(6*5)+(5*9)+(4*3)+(3*7)+(2*4)+(1*9)=125
125 % 10 = 5
So 5937-49-5 is a valid CAS Registry Number.

5937-49-5SDS

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 epigibberic acid

1.2 Other means of identification

Product number -
Other names 1,7β-Dimethyl-4bβ,5,6,7,9,10-hexahydro-7α,9aα-methano-benz<a>azulen-8-on- carbonsaeure-(10β)

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:5937-49-5 SDS

5937-49-5Downstream Products

5937-49-5Relevant articles and documents

A ring-distortion strategy to construct stereochemically complex and structurally diverse compounds from natural products

Huigens III, Robert W.,Morrison, Karen C.,Hicklin, Robert W.,Flood J.r., Timothy A.,Richter, Michelle F.,Hergenrother, Paul J.

, p. 195 - 202 (2013/05/09)

High-throughput screening is the dominant method used to identify lead compounds in drug discovery. As such, the makeup of screening libraries largely dictates the biological targets that can be modulated and the therapeutics that can be developed. Unfortunately, most compound-screening collections consist principally of planar molecules with little structural or stereochemical complexity, compounds that do not offer the arrangement of chemical functionality necessary for the modulation of many drug targets. Here we describe a novel, general and facile strategy for the creation of diverse compounds with high structural and stereochemical complexity using readily available natural products as synthetic starting points. We show through the evaluation of chemical properties (which include fraction of sp 3 carbons, ClogP and the number of stereogenic centres) that these compounds are significantly more complex and diverse than those in standard screening collections, and we give guidelines for the application of this strategy to any suitable natural product.

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