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N-[5-(1,2-dihydroxyethyl)-4-hydroxy-2-oxotetrahydrofuran-3-yl]acetamide, also known as a complex organic compound, is a derivative of acetamide with a unique structure. It features a tetrahydrofuran ring, which is a type of heterocyclic compound, and contains multiple hydroxyl groups that contribute to its hydrophilic properties. This chemical is characterized by its molecular formula and structure, which define its chemical and physical properties. While the specific applications or uses of N-[5-(1,2-dihydroxyethyl)-4-hydroxy-2-oxotetrahydrofuran-3-yl]acetamide (non-preferred name) are not detailed in the provided information, it is likely to be found in specialized chemical research or industrial processes due to its intricate structure.

5469-77-2

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5469-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5469-77-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5469-77:
(6*5)+(5*4)+(4*6)+(3*9)+(2*7)+(1*7)=122
122 % 10 = 2
So 5469-77-2 is a valid CAS Registry Number.

5469-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[5-(1,2-dihydroxyethyl)-4-hydroxy-2-oxooxolan-3-yl]acetamide

1.2 Other means of identification

Product number -
Other names 2-Acetamido-2-deoxy-D-galactono-1,4-lactone

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:5469-77-2 SDS

5469-77-2Relevant academic research and scientific papers

A NEW AND DIRECT ACCESS TO GLYCONO-1,4-LACTONES FROM GLYCOPYRANOSES BY REGIOSELECTIVE OXIDATION AND SUBSEQUENT RING RESTRICTION

Isaac, Isabelle,Stasik, Imane,Beaupere, Daniel,Uzan, Raoul

, p. 383 - 386 (2007/10/02)

Treatment of partially protected or unprotected carbohydrates with the RhH(PPh3)4-benzalacetone system leads exclusively to glycono-1,4-lactones by regioselective oxidation and subsequent ring restriction.

2-Acetamido-2-deoxyaldonolactones from sugar formazans

Zsoldos-Mady, Virag,Pinter, Istvan,Neszmelyi, Andras,Messmer, Andras,Perczel, Andras

, p. 85 - 96 (2007/10/02)

A new approach towards simple aldonic acid derivatives starting from the corresponding aldoses via the 2-acetamido-2-deoxy formazans resulted in the synthesis of 2-acetamido-2-deoxy-D-galactono-1,4-lactone (8), and its 6-deoxy (11) and 6-azido-6-deoxy (14) analogues on treatment with trifluoroacetic acid.The five-membered ring structure of the lactones and that of the intermediate lactone phenylhydrazone (7) was proved by 1H and 13C NMR studies, including deuterium-induced differential isotope shift (DIS) measurements.With sodium borohydride, lactones 8 and 11 were converted into 2-acetamido-2-deoxy-D-galactitol (15) and its 6-deoxy analogue (17), respectively.

Aldonhydroximo-lactones. Preparation and Determination of Configuration

Beer, Dieter,Vasella, Andrea

, p. 2254 - 2274 (2007/10/02)

The synthesis of the unprotected, (Z)-configurated hexon- and pentonhydroximo-lactones 2a-12a by oxidation of D-glucose, cellobiose, D-galactose, D-mannose, 2-acetamido-2-deoxy-D-glucose, D-ribose, and D-arabinose oxime with MnO2, Hg(OAc)2, or O2 in the p

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