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2-Acetylamino-2-deoxy-D-glucitol 1,3,4,5,6-pentaacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56211-19-9

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56211-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56211-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,1 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56211-19:
(7*5)+(6*6)+(5*2)+(4*1)+(3*1)+(2*1)+(1*9)=99
99 % 10 = 9
So 56211-19-9 is a valid CAS Registry Number.

56211-19-9SDS

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 2-acetamido-2-deoxy-D-glucitol pentaacetate

1.2 Other means of identification

Product number -
Other names (-)-Hexa-N,O-acetyl-D-glucosaminol

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:56211-19-9 SDS

56211-19-9Relevant academic research and scientific papers

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.

A STEREOSELECTIVE SYNTHESIS OF METHYL D-GLUCOSAMINATE VIA TIN(II) ENEDIOLATE FORMED FROM FURYLGLYOXAL

Mukaiyama, Teruaki,Tsuzuki, Ryuji,Kato, Jun-ichi

, p. 837 - 840 (2007/10/02)

The tin(II) enediolate, formed in situ from furyldlyoxal, reacts with polyoxyaldehydes such as 2,3-isopropylidene-D-glyceraldehyde and 4-O-benzyl-2,3-O-isopropylidene-L-threose to give the cross aldol adducts in good yields.This reaction is successfully a

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