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4860-15-5

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4860-15-5 Usage

General Description

Spirosol-5-en-3-ol,28-acetyl-, 3-acetate, (3b,22a,25R)- is a complex organic compound. It is a steroid derivative with a specific molecular structure, containing a cyclopentane ring and multiple functional groups including acetyl and acetate moieties. The compound exhibits stereochemistry with a 3b, 22a, 25R configuration. This chemical may have potential applications in pharmaceuticals or research due to its unique structure and potential biological activity. Understanding and studying the properties and potential uses of this compound could have implications for drug development and therapeutic interventions.

Check Digit Verification of cas no

The CAS Registry Mumber 4860-15-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,6 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4860-15:
(6*4)+(5*8)+(4*6)+(3*0)+(2*1)+(1*5)=95
95 % 10 = 5
So 4860-15-5 is a valid CAS Registry Number.

4860-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name solasodine N,O-diacetate

1.2 Other means of identification

Product number -
Other names O,N-Diacetyl-solasodin

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:4860-15-5 SDS

4860-15-5Relevant articles and documents

Copper-catalyzed 1,3-dipolar cycloaddition reaction of spirosolanederived azide for the preparation of modified solasodine alkaloid

Finke, Anastasiya O.,Mironov, Maxim E.,Skorova, Anna B.,Shults, Elvira E.

, p. 411 - 416 (2018)

[Figure not available: see fulltext.] Modification of the steroidal alkaloid solasodine was performed by introduction of 1,2,3-triazolyl substituents at the С-6 atom of spirosolane ring system. The azidolysis of 5,6α-epoxysolasodine diacetate, formed as the major product during epoxidation of solasodine diacetate by the action of sodium azide in DMF in the presence of ammonium chloride, proceeded through the formation of 6β-azido-5α-hydroxysolasodine diacetate. The newly obtained azide was used in reactions with terminal alkynes in the presence of copper(I) bromide and N,N-diisopropylethylamine in DMF to synthesize the respective (22R,25R)-N,O-diacetyl-6β-[4-aryl-1,2,3-triazol-1-yl]-5α-hydroxyspirosolanes.

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