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155544-65-3

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155544-65-3 Usage

Functional groups

acetamido group, two acetate groups
Lack of hydroxyl groups on 2 and 3 carbon positions
Six-carbon compound with a double bond (hex-2-en functionality)
Potential diverse chemical properties and applications in organic synthesis and medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 155544-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,5,4 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 155544-65:
(8*1)+(7*5)+(6*5)+(5*5)+(4*4)+(3*4)+(2*6)+(1*5)=143
143 % 10 = 3
So 155544-65-3 is a valid CAS Registry Number.

155544-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetamido-5,6-di-O-acetyl-2,3-didehydro-2,3-dideoxy-D-threo-hexono-1,4-lactone

1.2 Other means of identification

Product number -
Other names Acetic acid (R)-2-acetoxy-1-((R)-4-acetylamino-5-oxo-2,5-dihydro-furan-2-yl)-ethyl 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:155544-65-3 SDS

155544-65-3Relevant articles and documents

Malonofungin: an antifungal aminomalonic acid from Phaeoramularia fusimaculans.

Berova,Breinholt,Jensen,Kjaer,Lo,Nakanishi,Nielsen,Olsen,Pedersen,Stidsen

, p. 240 - 251 (2007/10/02)

In screening for antifungal metabolites, a novel compound, malonofungin, exhibiting growth inhibitory activity against Botrytis cinerea (grey mould), has been isolated from fermentations of Phaeoramularia fusimaculans CBS 616.87. Its structure is established as (E)-(3R,4S,5S)-5-acetoxy-2-amino-2-carboxy-3,4-dihydroxy-14-oxoicos++ +-6-enoic acid, representing an addition to the rare class of naturally occurring aminomalonic acids. 1H NMR data and extensive use of CD spectroscopy have been utilized to establish the absolute stereochemistry of malonofungin. The structural and biological relationship of malonofungin to previously reported fungal metabolites is discussed.

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