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28876-37-1

28876-37-1

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28876-37-1 Usage

Chemical Properties

Crystalline Solid

Check Digit Verification of cas no

The CAS Registry Mumber 28876-37-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28876-37:
(7*2)+(6*8)+(5*8)+(4*7)+(3*6)+(2*3)+(1*7)=161
161 % 10 = 1
So 28876-37-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO6/c1-3(11)9-5-6(13)7(4(12)2-10)15-8(5)14/h4-7,10,12-13H,2H2,1H3,(H,9,11)/t4-,5-,6+,7?/m1/s1

28876-37-1SDS

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 2-Acetamido-2-deoxy-D-mannono-1,4-lactone

1.2 Other means of identification

Product number -
Other names N-[(3S,4R,5S)-5-[(1R)-1,2-dihydroxyethyl]-4-hydroxy-2-oxooxolan-3-yl]acetamide

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:28876-37-1 SDS

28876-37-1Relevant articles and documents

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Pravdic

, p. 471 (1970)

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Synthesis of sphingosine relatives, XXI. - Synthesis of sphingofungin D and its three diastereomers

Otaka, Ken,Mori, Kenji

, p. 1795 - 1802 (2007/10/03)

Sphingofungin D [(2S,3R,4R,5S,14R)-1] and its three diastereomers were synthesized by starting from (R)-1,2 epoxyoctane [(R)-7], 1-heptyne (8) and N-acetyl-D-mannosamine (9).

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.

The oxidation of partially substituted 2-acetamido-2-deoxyaldoses with methyl sulfoxide-acetic anhydride. Some 2-acetamido-2-deoxyaldonic acid derivatives.

Pravdic,Fletcher Jr.

, p. 353 - 364 (2007/10/11)

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