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89067-86-7

allyl 3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89067-86-7 Structure

  • Basic information

    1. Product Name: allyl 3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
    2. Synonyms: allyl 3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
    3. CAS NO:89067-86-7
    4. Molecular Formula:
    5. Molecular Weight: 439.465
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89067-86-7.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: allyl 3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: allyl 3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside(89067-86-7)
    11. EPA Substance Registry System: allyl 3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside(89067-86-7)

  • 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: 89067-86-7(Hazardous Substances Data)

89067-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89067-86-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,6 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89067-86:
(7*8)+(6*9)+(5*0)+(4*6)+(3*7)+(2*8)+(1*6)=177
177 % 10 = 7
So 89067-86-7 is a valid CAS Registry Number.

89067-86-7Downstream Products

89067-86-7Relevant articles and documents

Chemical Synthesis of Nod-Rm-1: the Nodilation Factor Involved in Rhizobium meliloti-legume Symbiosis

Wang, Lai-Xi,Li, Chuan,Wang, Qin-Wei,Hui, Yong-Zheng

, p. 621 - 628 (2007/10/02)

A total synthesis of the sulfated lipotetrasaccharide (NodRm-1) is described.First, the disaccharide glycosyl donor - O-(2-azido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl chloride 3a or

SYNTHESIS OF STRUCTURAL ELEMENTS OF THE CAPSULAR POLYSACCHARIDE OF STREPTOCOCCUS PNEUMONIAE TYPE 14

Koeman, Franciscus A. W.,Meissner, Johannes W. G.,Ritter, Hendrik R. P. van,Kamerling, Johannis P.,Vliegenthart, Johannes F. G.

, p. 1 - 26 (2007/10/02)

The synthesis is reported of methyl O-β-D-galactopyranosyl-(1->4)-O-β-D-glucopyranosyl-(1->6)-O-4)>-O-2-acetamido-2-deoxy-β-D-glucopyranoside (13), methyl O-β-D-galactopyranosyl-(1->4)-O-β-D-glucopyranosyl-(1->6)-O-4)>-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->3)-O-β-D-galactopyranosyl-(1->4)-β-D-glucopyranoside (28), and O-β-D-galactopyranosyl-(1->4)-O-β-D-glucopyranosyl-(1->6)-O-4)>-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->3)-O-β-D-galactopyranosyl-(1->4)-D-glucopyranose (38), representing fragments of the capsular polysaccharide of Streptococcus pneumoniae type 14 (3)-β-D-Galp-(1->4)-β-D-Glcp-(1->6)-4)>-β-D-GlcpNAc-(1->>n). 4-O-(2,3,4,6-Tetra-O-acetyl-β-D-galactopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl trichloroacetamidate (6) was coupled regio- and stereoselectively with HO-6 of methyl 3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (4) in dichloromethane, using boron trifluoroetherate as a promoter.Coupling of 2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl trichloroacetimidate (8) with HO-4 of the resulting trisaccharide derivative (9) in dichloromethane, using boron trifluoroetherate as a promoter, afforded methyl 4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-6-O--3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (10).Debenzylation of 10, followed by dephthaloylation, N,O-acetylation, and de-O-acetylation gave tetrasaccharide methyl glycoside 13.Disaccharide derivative 6 was also coupled with HO-6 of allyl 3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (16) in dichloromethane using trimethylsilyl trifluoromethanesulfonate as a promoter.Coupling of 8 with HO-4 of the resulting trisaccharide derivative (17) in dichloromethane, using trimethylsilyl trifluoromethanesulfonate as a promoter, afforded allyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-6-O--3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (18).Deallylation of 18, followed by imidation gave an activated tetrasaccharide (20), which was coupled to both methyl (24) and benzyl (33) 2,3,6-tri-O-benzyl-4-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-β-D-glucopyranoside in dichloromethane, using trimethylsilyl trifluoromethanesulfonate as a promoter, to give the corresponding hexasaccharide derivatives 25 and 34.Debenzylation of 25, followed by dephthaloylation, N,O-acetylation, and de-O-acetylation gave hexasaccharide methyl glycoside 28.Dephthaloylation of 34, followed by N,O-acetylation, debenzylation, re-O-acetylation and de-O-acetylation gave hexasaccharide 38.

Synthesis of an appropriately protected core glycotetraoside, a key intermediate for the synthesis of "bisected" complex-type glycans of a glycoprotein.

Yamazaki,Kitajima,Nukada,Ito,Ogawa

, p. 15 - 30 (2007/10/02)

A stereocontrolled synthetic route to a glycotetraoside, allyl O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranosyl)-(1--- -4)-O- (3,6-di-O-allyl-2-O-benzyl-beta-D-mannopyranosyl)-(1----4)-O-3, 6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-gluco

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