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1-Bromoacetamido-1-deoxy-β-D-galactopyranose, also known as N-acetyl-D-galactosamine, is a crystalline chemical compound with the molecular formula C8H15BrNO6. It is derived from D-galactose and contains a bromoacetamide group, making it useful for labeling and modification of carbohydrates. Its properties and structure make it suitable for various applications in organic chemistry and biochemistry research.

33758-19-9

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33758-19-9 Usage

Uses

Used in Organic Chemistry Research:
1-BROMOACETAMIDO-1-DEOXY-B-D-GALACTOPYRA NOSE CRYST is used as a chemical intermediate for the synthesis of glycosidic compounds, which are important in the development of various organic compounds.
Used in Biochemistry Research:
1-BROMOACETAMIDO-1-DEOXY-B-D-GALACTOPYRA NOSE CRYST is used as a substrate for enzyme assays, allowing researchers to study the activity and properties of enzymes involved in carbohydrate metabolism and other biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 33758-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,5 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33758-19:
(7*3)+(6*3)+(5*7)+(4*5)+(3*8)+(2*1)+(1*9)=129
129 % 10 = 9
So 33758-19-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H14BrNO6/c9-1-4(12)10-8-7(15)6(14)5(13)3(2-11)16-8/h3,5-8,11,13-15H,1-2H2,(H,10,12)

33758-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-N-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]acetamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:33758-19-9 SDS

33758-19-9Downstream Products

33758-19-9Relevant academic research and scientific papers

An improved procedure for the synthesis of N-bromoacetyl-β- glycopyranosylamines, derivatives of mono- and disaccharides

Likhosherstov,Novikova,Zheltova,Shibaev

, p. 709 - 713 (2007/10/03)

An improved procedure for the synthesis of N-bromoacetyl-β- glycopyranosylamines from the corresponding β-glycosylamines was developed. The procedure is applicable to a wide range of derivatives of monosaccharides (hexoses, 2-acetamido-2-deoxyhexoses, hexuronamides, and 6-deoxyhexoses) and some disaccharides. For the derivatives of pentoses and 2-deoxyhexoses, the use of the corresponding β-glycosylammonium carbamates was found to be more convenient. N-Bromoacetyl-β-glycopyranosylamines derived from D-mannose, L-rhamnose, D-glucuronamide, 2-deoxy-D-arabino-hexose, 2-deoxy-D-lyxo-hexose, and melibiose were obtained for the first time.

Chemoselective elaboration of O-linked glycopeptide mimetics by alkylation of 3-thioGalNAc

Marcaurelle,Bertozzi

, p. 1587 - 1595 (2007/10/03)

A critical branch point in mucin-type oligosaccharides is the β1 → 3 glycosidic linkage to the core α-N-acetylgalactosamine (GalNAc) residue. We report here a strategy for the synthesis of O-linked glycopeptide analogues that replaces this linkage with a

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