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5508-47-4

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5508-47-4 Usage

Uses

Gibberellin A7 Methyl Ester is a derivative of Gibberellin A7 (G377460), a plant hormone that was isolated from culture filtrates of the fungus Gibberella fujikuroi. Gibberellin A7 was shown to promote the growth and elongation of cells.

Check Digit Verification of cas no

The CAS Registry Mumber 5508-47-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5508-47:
(6*5)+(5*5)+(4*0)+(3*8)+(2*4)+(1*7)=94
94 % 10 = 4
So 5508-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C23H28ClN3O3/c1-4-21(28)27-15-13-26(14-16-27)19-9-7-18(8-10-19)25-22(29)23(2,3)30-20-11-5-17(24)6-12-20/h5-12H,4,13-16H2,1-3H3,(H,25,29)

5508-47-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenoxy)-2-methyl-N-[4-(4-propanoylpiperazin-1-yl)phenyl]propanamide

1.2 Other means of identification

Product number -
Other names gibberellin A7 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:5508-47-4 SDS

5508-47-4Downstream Products

5508-47-4Relevant articles and documents

Substitution Reactions of the 3-Epimeric Methanesulphonates of Methyl Gibberellate

Duri, Zvitendo J.,Hanson, James R.

, p. 603 - 607 (2007/10/02)

Whereas displacement of the 3β-(axial)-methylsulphonyloxy group from methyl gibberellate with lithium chloride or buffered aqueous acetone proceeds predominantly with syn rearrangement to afford the 1β-chloro- or 1β-hydroxy-gibberellin, the corresponding 3α-(equatorial) epimer reacts with simple inversion of configuration.This affords on the one hand a facile route to the 1-hydroxygibberellins and, on the other, a means of labelling gibberellins at C-3.

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