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D-fucosylamine, also known as 6-deoxy-L-galactose, is a monosaccharide that is structurally similar to galactose but lacks an oxygen atom at the sixth carbon position. It is a component of various natural products, including fucose-containing glycans and glycoconjugates, which play crucial roles in cell recognition, adhesion, and signaling processes. D-fucosylamine is an important building block in the synthesis of complex carbohydrates and is used in the development of pharmaceuticals, vaccines, and diagnostic tools. Its unique structure and properties make it a valuable compound for research and applications in the fields of chemistry, biology, and medicine.

6931-59-5

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6931-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6931-59-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6931-59:
(6*6)+(5*9)+(4*3)+(3*1)+(2*5)+(1*9)=115
115 % 10 = 5
So 6931-59-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO4/c1-2-4(8)5(9)3(7)6(10)11-2/h2-6,8-10H,7H2,1H3/t2-,3-,4+,5-,6?/m1/s1

6931-59-5SDS

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 (3R,4S,5R,6R)-2-amino-6-methyloxane-3,4,5-triol

1.2 Other means of identification

Product number -
Other names D-Fucosylamine

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:6931-59-5 SDS

6931-59-5Downstream Products

6931-59-5Relevant academic research and scientific papers

Structure of the O-antigen of Acinetobacter lwoffii EK30A; Identification of d-homoserine, a novel non-sugar component of bacterial polysaccharides

Arbatsky, Nikolay P.,Kondakova, Anna N.,Shashkov, Alexander S.,Drutskaya, Marina S.,Belousov, Pavel V.,Nedospasov, Sergei A.,Petrova, Mayya A.,Knirel, Yuriy A.

experimental part, p. 3571 - 3577 (2010/08/21)

We established a peculiar structure of the O-specific polysaccharide (O-antigen) of a psychrotrophic strain of Acinetobacter lwoffii, EK30A, isolated from a 1.6-1.8 million-year-old Siberian permafrost subsoil sediment sample. The polysaccharide was released by mild acid degradation of the lipopolysaccharide and studied using chemical analyses, Smith degradation, 1H and 13C NMR spectroscopy and mass spectrometry. It was found to contain d-homoserine, which is N-linked to 4-amino-4,6-dideoxy-d- glucose (Qui4N) and is N-acylated itself with acetyl in about half of the repeating units or (S)-3-hydroxybutanoyl group in the other half. The following is the structure of the tetrasaccharide repeating unit of the polysaccharide: →3)-β-d-Quip4NAcyl-(1→6)-α-d-Galp-(1→4) -α-d-GalpNAc-(1→3)-α-d-FucpNAc-(1→ where Acyl stands for either N-acetyl- or N-[(S)-3-hydroxybutanoyl]-d-homoseryl. The Royal Society of Chemistry 2010.

Identification and role of a 6-deoxy-4-keto-hexosamine in the lipopolysaccharide outer core of yersinia enterocolitica serotype O:3

Pinta, Elise,Duda, Katarzyna A.,Hanuszkiewicz, Anna,Kaczynski, Zbigniew,Lindner, Buko,Miller, Wayne L.,Hyytiaeinen, Heidi,Vogel, Christian,Borowski, Sabine,Kasperkiewicz, Katarzyna,Lam, Joseph S.,Radziejewska-Lebrecht, Joanna,Skurnik, Mikael,Holst, Otto

supporting information; experimental part, p. 9747 - 9754 (2010/08/06)

The outer core (OC) region of Yersinia enterocolitica serotype 0:3 lipopolysaccharide is a hexasaccharide essential for the integrity of the outer membrane. It is involved in resistance against cationic antimicrobial peptides and plays a role in virulence

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