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6082-22-0

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6082-22-0 Usage

Chemical Properties

White Solid

Uses

Methyl N-Acetyl-2-deoxy-α-D-galactosamine can be used for antibody to detect epiglycanin-?related glycoproteins in body fluids of cancer patients.

Definition

ChEBI: An N-acetyl-alpha-D-galactosaminide having a methyl substituent at the anomeric position.

Check Digit Verification of cas no

The CAS Registry Mumber 6082-22-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6082-22:
(6*6)+(5*0)+(4*8)+(3*2)+(2*2)+(1*2)=80
80 % 10 = 0
So 6082-22-0 is a valid CAS Registry Number.

6082-22-0 Well-known Company Product Price

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  • Aldrich

  • (766690)  Methyl 2-acetamido-2-deoxy-α-D-galactopyranoside  

  • 6082-22-0

  • 766690-250MG

  • 2,302.56CNY

  • Detail
  • Aldrich

  • (766690)  Methyl 2-acetamido-2-deoxy-α-D-galactopyranoside  

  • 6082-22-0

  • 766690-1G

  • 5,914.35CNY

  • Detail

6082-22-0SDS

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 methyl N-acetyl-α-D-galactosaminide

1.2 Other means of identification

Product number -
Other names methyl N-acetyl-alpha-D-galactosaminide

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:6082-22-0 SDS

6082-22-0Relevant articles and documents

Design, physico-chemical characterization andin vitrobiological activity of organogold(iii) glycoconjugates

Pettenuzzo, Andrea,Vezzù, Keti,Di Paolo, Maria Luisa,Fotopoulou, Eirini,Marchiò, Luciano,Via, Lisa Dalla,Ronconi, Luca

supporting information, p. 8963 - 8979 (2021/07/02)

To develop new metal-based glycoconjugates as potential anticancer agents, four organometallic gold(iii)-dithiocarbamato glycoconjugates of the type [AuIII(2-Bnpy)(SSC-Inp-GlcN)](PF6) (2-Bnpy: 2-benzylpyridine; Inp: isonipecotic moie

Ultrasonication-Assisted Synthesis of a d-Glucosamine-Based β-CD Inclusion Complex and Its Application as an Aqueous Heterogeneous Organocatalytic System

Rani, Dhiraj,Sethi, Aaftaab,Kaur, Khushwinder,Agarwal, Jyoti

, p. 9548 - 9557 (2020/09/09)

For the first time, an inclusion complex has been crafted between a carbohydrate-based molecule and a β-cyclodextrin (CD) hydrophobic cavity for asymmetric catalytic applications. This novel d-glucosamine-based inclusion compound has been synthesized in h

Selective anomeric acetylation of unprotected sugars in water

Lim, David,Fairbanks, Antony J.

, p. 1896 - 1900 (2017/03/09)

High yielding selective acetylation of only the anomeric hydroxyl of unprotected sugars is possible in aqueous solution using 2-chloro-1,3-dimethylimidazolinium chloride (DMC), thioacetic acid, and a suitable base. The reaction, which may be performed on a multi-gram scale, is stereoselective for sugars that possess a hydroxyl group at position-2, exclusively yielding the 1,2-trans products. The use of an iterative reagent addition procedure allows the use of sodium carbonate as the base, avoiding the formation of triethylammonium salts, which may hamper product purification. The glycosyl acetate products may be used as donor substrates for glycosidase-catalysed synthesis. The crude aqueous acetylation reaction mixture may also be used for this purpose.

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