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AM toxin III is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57765-94-3

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57765-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57765-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,6 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57765-94:
(7*5)+(6*7)+(5*7)+(4*6)+(3*5)+(2*9)+(1*4)=173
173 % 10 = 3
So 57765-94-3 is a valid CAS Registry Number.
InChI:InChI=1/C22H29N3O6/c1-12(2)18-21(29)25-17(7-5-6-15-8-10-16(26)11-9-15)20(28)23-13(3)19(27)24-14(4)22(30)31-18/h8-12,14,17-18,26H,3,5-7H2,1-2,4H3,(H,23,28)(H,24,27)(H,25,29)

57765-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name AM-toxin III

1.2 Other means of identification

Product number -
Other names 9-[3-(4-Hydroxy-phenyl)-propyl]-12-isopropyl-3-methyl-6-methylene-1-oxa-4,7,10-triaza-cyclododecane-2,5,8,11-tetraone

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:57765-94-3 SDS

57765-94-3Downstream Products

57765-94-3Relevant academic research and scientific papers

SYNTHESES OF AM-TOXIN III AND ITS ANALOGS USING THE HOFMANN DEGRADATION

Kanmera, Tatsuhiko,Aoyagi, Haruhiko,Waki, Michinori,Kato, Tetsuo,Izumiya, Nobuo,et al.

, p. 3625 - 3628 (2007/10/02)

Syntheses of cyclotetradepsipeptides, AM-toxin III and two analogs, were achieved, in which the Hofmann degradation method was used in order to derive a dehydroalanine residue from a 2,3-diamiopropionic acid residue in cyclodepsipeptide presursors.

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