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N-((4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 95341-97-2 Structure
  • Basic information

    1. Product Name: N-((4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-acetamide
    2. Synonyms:
    3. CAS NO:95341-97-2
    4. Molecular Formula:
    5. Molecular Weight: 235.237
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95341-97-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-((4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-((4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-acetamide(95341-97-2)
    11. EPA Substance Registry System: N-((4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-acetamide(95341-97-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 95341-97-2(Hazardous Substances Data)

95341-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95341-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,4 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 95341-97:
(7*9)+(6*5)+(5*3)+(4*4)+(3*1)+(2*9)+(1*7)=152
152 % 10 = 2
So 95341-97-2 is a valid CAS Registry Number.

95341-97-2Relevant articles and documents

Preparation and Properties of New Surfactants Containing D-Glucosamine as the Building Block

Kida, Toshiyuki,Yurugi, Keiji,Masuyama, Araki,Nakatsuji, Yohji,Ono, Daisuke,Takeda, Tokuji

, p. 773 - 780 (1995)

Three types of new surfactants were prepared by using N-acetyl-D-glucosamine as a starting material.The first type of surfactant, sodium methyl 4,6-O-alkylidene-2-(carboxylatomethylamino)-2-deoxy-D-glucopyranoside, was prepared successively by the following treatments: methyl glucosidation of N-acetyl-D-glucosamine, transacetalization with an appropriate aldehyde dimethyl acetal, deacetylation, and finally reaction of the resulting methyl-4,6-O-alkylidene-2-amino-2-deoxy-D-glucopyranoside (2-amino precursor) with bromoacetic acid.The reaction of this 2-amino precursor with methyl iodide yielded the second type of surfactant, methyl 4,6-O-alkylidene-2-deoxy-2(trimethylammonio)-D-glucopyranoside iodide, in excellent yield.The last type of compound, sodium methyl 2-acetamide-4,6-O-alkylidene-3-O--2-deoxy-D-glucopyranoside, was synthesized by the reaction of methyl 2-acetamide-4,6-O-alkylidene-2-deoxy-D-glucopyranoside with 2-chloropropionic acid.Concerning the two carboxylate types of surfactants, the compounds containing a C9 or C11 hydrophobic chain in the alkylidene part showed higher water solubility than the corresponding compounds containing a C7 hydrophobic chain.Both the micelle-forming property and the ability to lower the surface tension of these carboxylate types of compounds increased with an increase in the length of the hydrophobic chain in the alkylidene part.These compounds can be applied to new acid-decomposable types of cleavable surfactants because they contain an acetal group.The acetal bond of the ammonium type of compound was cleaved more slowly than that of the corresponding carboxylate types of surfactants in 2percent aqueous HCl solution.The biodegradabilities of these compounds were also determined.KEY WORDS: Acetalization, acid decomposition properties, biodegradability, D-glucosamine, surface-active properties.

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

Synthetic development of sugar amino acid oligomers towards novel podophyllotoxin analogues

Bouchard, Megan,Tremblay, Thomas,Paré-Lacroix, Marie-Pier,Gagné-Boulet, Mathieu,Fortin, Sébastien,Giguère, Denis

, (2021/11/30)

In this work, we have developed an approach for the synthesis of sugar amino acid oligomers based on the glucosamine scaffold. We found that the solid-phase approach was unsuccessful for the preparation of sugar amino acid oligomers and the limitation of

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

Ring-Opening Reactions of the N-4-Nosyl Hough-Richardson Aziridine with Nitrogen Nucleophiles

Ru?il, Tomá?,Trávní?ek, Zdeněk,Canka?, Petr

, p. 723 - 730 (2017/04/26)

Dinosylated α-d-glucopyranoside was directly transformed into α-d-altropyranosides via in situ formed N-4-nosyl Hough-Richardson aziridine with nitrogen nucleophiles under mild conditions in fair to excellent yields. The scope of the aziridine ring-opening reaction was substantially broadened contrary to the conventional methods introducing solely the azide anion at high temperatures. If necessary, the N-4-nosyl Hough-Richardson aziridine can be isolated by filtration in a very good yield and high purity.

Sugar derived alkamine catalytic imine reduction method

-

Paragraph 0035; 0036; 0037, (2016/10/07)

The invention discloses a method used for catalytic reduction of imine with saccharide-derivatized amino alcohol. According to the method, imine is taken as a substrate. The method comprises following steps: 1) imine and saccharide-derivatized amino alcohol are dissolved in an organic solvent I, wherein molar ratio of imine to saccharide-derivatized amino alcohol ranges from 100:1-20; 2) trichlorosilane with 1.5 to 5 times equivalent weights is added into a solution obtained via step 1) dropwise, an obtained mixture is stirred and reacted for 12 to 36h at a temperature of -20 to 40 DEG C, and a saturated sodium bicarbonate solution is used for quenching; 3) a material obtained via step 2) is extracted with an organic solvent II, and is subjected to column chromatography isolation so as to obtain amine compounds.

Synthetic heparin pentasaccharides

-

Page/Page column 36; 37, (2016/02/12)

Preparation and use of synthetic monosaccharides, disaccharides, trisaccharides, tetrasaccharides and pentasaccharides useful for the preparation of synthetic heparinoids.

N-acetylgalactosamine green synthetic method

-

Paragraph 0037; 0038, (2016/11/28)

The present invention discloses a N-acetylgalactosamine green synthetic method. According to the method, N-acetylglucosamine as a raw material is successively condensed with an alcohol and pivaloyl chloride, and then N-acetylgalactosamine can be obtained

Glucosamine-based primary amines as organocatalysts for the asymmetric aldol reaction

Agarwal, Jyoti,Peddinti, Rama Krishna

scheme or table, p. 3502 - 3505 (2011/06/21)

Glucosamine derivatives have been synthesized starting from commercially available N-acetyl-D-glucosamine/glucosamine hydrochloride and have been employed successfully as efficient organocatalysts for the direct asymmetric aldol reaction between cyclohexa

Oligo-Aminosaccharide compound

-

Page/Page column 8, (2011/01/12)

An oligo-aminosaccharide compound formed by binding 3 to 6 saccharides, such as 2,6-diamino-2,6-dideoxy-α-(1→4)-D-glucopyranose oligomers, or a salt thereof, which has high affinity to a double-stranded nucleic acid.

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