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2,3,4-tri-O-acetyl-6-O-(p-tolylsulfonyl)-α-D-galactosyl bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13046-90-7 Structure
  • Basic information

    1. Product Name: 2,3,4-tri-O-acetyl-6-O-(p-tolylsulfonyl)-α-D-galactosyl bromide
    2. Synonyms: 2,3,4-tri-O-acetyl-6-O-(p-tolylsulfonyl)-α-D-galactosyl bromide
    3. CAS NO:13046-90-7
    4. Molecular Formula:
    5. Molecular Weight: 523.356
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13046-90-7.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: 2,3,4-tri-O-acetyl-6-O-(p-tolylsulfonyl)-α-D-galactosyl bromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4-tri-O-acetyl-6-O-(p-tolylsulfonyl)-α-D-galactosyl bromide(13046-90-7)
    11. EPA Substance Registry System: 2,3,4-tri-O-acetyl-6-O-(p-tolylsulfonyl)-α-D-galactosyl bromide(13046-90-7)
  • 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: 13046-90-7(Hazardous Substances Data)

13046-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13046-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,4 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13046-90:
(7*1)+(6*3)+(5*0)+(4*4)+(3*6)+(2*9)+(1*0)=77
77 % 10 = 7
So 13046-90-7 is a valid CAS Registry Number.

13046-90-7Relevant articles and documents

Selection of a synthetic glycan oligomer from a library of DNA-templated fragments against DC-SIGN and inhibition of HIV gp120 binding to dendritic cells

Ciobanu, Mihai,Huang, Kuo-Ting,Daguer, Jean-Pierre,Barluenga, Sofia,Chaloin, Olivier,Schaeffer, Evelyne,Mueller, Christopher G.,Mitchell, Daniel A.,Winssinger, Nicolas

supporting information; scheme or table, p. 9321 - 9323 (2011/10/09)

We report the synthesis of a nucleic acid-encoded carbohydrate library, its combinatorial self-assembly into 37485 pairs and a screen against DC-SIGN leading to the identification of consensus ligand motifs. A prototypical example from the selected pairs

Novel cyclic tetraselenides of mannose: synthesis and mechanistic studies

Sivapriya, Kirubakaran,Suguna, Perumal,Chandrasekaran, Srinivasan

, p. 2091 - 2095 (2008/02/04)

In this Letter, we disclose the synthesis of novel cyclic tetraselenides starting from mannose which are very unusual and rare and have been synthesised for the first time. The structures are confirmed by X-ray analysis. The reactivity of the reagent tetr

Synthesis of 6-amino-1,6-anhydro-6-deoxysugar derivatives

Lafont, Dominique,Wollny, Andreas,Boullanger, Paul

, p. 9 - 16 (2007/10/03)

Staudinger reaction of triphenylphosphine with 2,3,4-tri-O-acetyl-6-O-p-tolylsulfonyl-β-d-glycopyranosyl azides led to an anomeric iminophosphorane which rearranged in situ by elimination of the sulfonate at C-6. The 1,6-anhydro-6-deoxy-6-triphenylphospho

Structure-Activity Relationships of β-D-(2S,5R)- and α-D-(2S,5S)-1,3-oxathiolanyl Nucleosides as Potential Anti-HIV Agents

Jeong, Lak S.,Schinazi, Raymond F.,Beach, J. Warren,Kim, Hea O.,Shanmuganathan, Kirupathevy,et al.

, p. 2627 - 2638 (2007/10/02)

The β-D-(2S,5R)- and α-D-(2S,5S)-1,3-oxathiolanylpyrimidine and -purine nucleosides with natural nucleoside configuration were synthesized and evaluated against HIV-1 in human peripheral blood mononuclear (PBM) cells.The key intermediate 14, which was uti

Efficient and stereoselective synthesis of methyl 3-O-(3,6-anhydro-β-D-galactopyranosyl)-α-D-galactopyranoside and methyl 3,6-anhydro-4-O-β-D-galactopyranosyl-α-D-galactopyranoside

Rashid,Mackie

, p. 147 - 155 (2007/10/02)

Methyl 3-O-(3,6-anhydro-β-D-galactopyranosyl)-α-D-galactopyranoside (3) and methyl 3,6-anhydro-4-O-β-D-galactopyranosyl-α-D-galactopyranoside (4) have been synthesised stereoselectively using three coupling procedures. Acceptable yields were achieved usin

Enantiomeric Synthesis of (+)-BCH-189 cytosine> from D-Mannose and Its Anti-HIV Activity

Chu, Chung K.,Beach, J. Warren,Jeong, Lak S.,Choi, Bo G.,Comer, Frank I.,et al.

, p. 6503 - 6505 (2007/10/02)

Enantiomerically pure (+)-BCH-189 has been synthesized from D-mannose via 1,6-thioanhydro-D-mannose and its anti-HIV activity has been determined in peripheral blood mononuclear cells.

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