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87028-22-6

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87028-22-6 Usage

Source

Synthetic chemical compound derived from stigmasterol

Structure

Fluorinated derivative with a fluorine atom replacing a hydrogen on the sterol ring structure

Pharmacological Activities

Anti-inflammatory properties
Antitumor properties

Experimental Findings

Inhibition of cancer cell growth
Reduction of inflammation in experimental models

Biological Functions

Potential cholesterol-lowering activity
Potential antioxidant activity

Further Research

Required to fully characterize its potential uses and mechanisms of action

Check Digit Verification of cas no

The CAS Registry Mumber 87028-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,0,2 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87028-22:
(7*8)+(6*7)+(5*0)+(4*2)+(3*8)+(2*2)+(1*2)=136
136 % 10 = 6
So 87028-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C29H47FO/c1-19(2)21(14-17-30)7-6-20(3)25-10-11-26-24-9-8-22-18-23(31)12-15-28(22,4)27(24)13-16-29(25,26)5/h6-8,19-21,23-27,31H,9-18H2,1-5H3/b7-6+/t20-,21+,23+,24+,25-,26+,27+,28+,29-/m1/s1

87028-22-6SDS

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 (3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-(2-fluoroethyl)-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1.2 Other means of identification

Product number -
Other names 29-Fluorostigmasterol

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:87028-22-6 SDS

87028-22-6Downstream Products

87028-22-6Relevant articles and documents

SYNTHESIS OF 29-FLUOROPHYTOSTEROLS: A NOVEL CLASS OF INSECT-ACTIVATED SELECTIVE POISONS

Prestwich, Glenn D.,Phirwa, Seloka

, p. 2461 - 2464 (1983)

Four 29-monofluorophytosterols are prepared from stigmasterol.When fed to insects, evidence is obtained for fluoroacetate poisoning via dealkylation at C-24.

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