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4550-88-3

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4550-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4550-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,5 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4550-88:
(6*4)+(5*5)+(4*5)+(3*0)+(2*8)+(1*8)=93
93 % 10 = 3
So 4550-88-3 is a valid CAS Registry Number.

4550-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-hydroxy-lupanoic acid-(28)-methyl ester

1.2 Other means of identification

Product number -
Other names 3β-3-hydroxylupan-28-oic acid methyl ester

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:4550-88-3 SDS

4550-88-3Downstream Products

4550-88-3Relevant articles and documents

Synthesis of oxadiazole derivative of pentacyclic triterpenoid and its biological activity

Rasul, Mohammed Golam

, p. 1143 - 1147 (2019/07/12)

Triterpenoid betunilic acid is extracted from outer bark of Biscofia javanica blume from Darjeeling hilly region and carried out transformative reaction to introduce oxadiazole moiety to ring A of the triterpenoid which was identified as 28-carbomethoxy lupan (2,3-c)-1′,2′,5′-oxadiazole. The derivative obtained has been selected for its antibacterial and fungicidal activity at different concentrations with respect to the parent compound. The structures of these compounds were established based on spectroscopic (UV, IR, NMR) analysis.

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