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10486-91-6

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10486-91-6 Usage

Description

2-ACETAMIDO-2-DEOXY-D-GALACTITOL, also known as a 2-deoxyhexitol derivative, is a chemical compound derived from galactitol. In this molecule, the 2-hydroxy substituent is replaced by an acetamido group, which gives it unique properties and potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a therapeutic agent for its unique chemical properties and potential to interact with biological systems.
Used in Chemical Research:
In the field of chemical research, 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a research compound for studying the effects of the acetamido group substitution on the properties and reactivity of galactitol derivatives. The expression is: 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a research compound for investigating the influence of acetamido group substitution on galactitol derivatives.
Used in Material Science:
2-ACETAMIDO-2-DEOXY-D-GALACTITOL may also find applications in material science, particularly in the development of novel materials with specific properties due to the presence of the acetamido group. The expression is: 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a building block for the development of new materials with unique properties in material science.
Please note that the provided materials do not specify any particular application for 2-ACETAMIDO-2-DEOXY-D-GALACTITOL, so the uses listed above are inferred based on the general properties of similar compounds and their potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 10486-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10486-91:
(7*1)+(6*0)+(5*4)+(4*8)+(3*6)+(2*9)+(1*1)=96
96 % 10 = 6
So 10486-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO6/c1-4(12)9-5(2-10)7(14)8(15)6(13)3-11/h5-8,10-11,13-15H,2-3H2,1H3,(H,9,12)/t5-,6+,7+,8-/m0/s1

10486-91-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-acetyl-D-galactosaminitol

1.2 Other means of identification

Product number -
Other names GalNAc-ol

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:10486-91-6 SDS

10486-91-6Relevant articles and documents

Perry,Webb

, p. 2481,2483 (1968)

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 MECHANISTIC CONSIDERATION OF THE HYDRAZINOLYSIS OF 3-O-SUBSTITUTED 2-ACETAMIDO-2-DEOXY-D-HEXOPYRANOSYL AND -D-HEXITOL RESIDUES IN THE ABSENCE AND PRESENCE OF HYDRAZINIUM SULFATE

Inoue, Yasuo,Kitajima, Ken

, p. 342 - 348 (2007/10/02)

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