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4-METHOXYPHENYL 3-O-ALLYL-2-AZIDO-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is a complex azido derivative of 2-deoxy-beta-D-glucopyranoside, featuring a 4-methoxyphenyl group at the 4-position, an allyl group at the 3-position, and a benzylidene acetal at the 4,6-positions. 4-METHOXYPHENYL 3-O-ALLYL-2-AZIDO-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSIDE holds potential in medicinal chemistry and pharmaceuticals due to its unique structural features, making it a valuable building block in organic chemistry and drug discovery.

889453-78-5

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  • (4aR,6S,7R,8R,8aS)-7-azido-6-(4-methoxyphenoxy)-2-phenyl-8-(prop-2-en-1-yloxy)-hexahydro-2H-pyrano[3,2-d][1,3]dioxine

    Cas No: 889453-78-5

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  • 4-Methoxyphenyl 3-O-Allyl-2-azido-4,6-O-benzylidene-2-deoxy-beta-D-glucopyranoside

    Cas No: 889453-78-5

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889453-78-5 Usage

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Used in Medicinal Chemistry:
4-METHOXYPHENYL 3-O-ALLYL-2-AZIDO-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a key intermediate in the synthesis of complex organic molecules and pharmaceuticals, leveraging its unique structural features for drug development.
Used in Chemical Biology:
In the field of chemical biology, 4-METHOXYPHENYL 3-O-ALLYL-2-AZIDO-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is utilized for bioorthogonal labeling and imaging, taking advantage of its azido group for selective chemical reactions within biological systems.
Used in Drug Synthesis:
4-METHOXYPHENYL 3-O-ALLYL-2-AZIDO-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSIDE serves as a building block in the creation of novel drug candidates, with its 4-methoxyphenyl and benzylidene groups offering potential for modification and optimization of therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 889453-78-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,9,4,5 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 889453-78:
(8*8)+(7*8)+(6*9)+(5*4)+(4*5)+(3*3)+(2*7)+(1*8)=245
245 % 10 = 5
So 889453-78-5 is a valid CAS Registry Number.
InChI:InChI=1/C23H25N3O6/c1-3-13-28-21-19(25-26-24)23(30-17-11-9-16(27-2)10-12-17)31-18-14-29-22(32-20(18)21)15-7-5-4-6-8-15/h3-12,18-23H,1,13-14H2,2H3/t18-,19-,20-,21-,22-,23-/m1/s1

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  • TCI America

  • (M1638)  4-Methoxyphenyl 3-O-Allyl-2-azido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside  >98.0%(HPLC)

  • 889453-78-5

  • 1g

  • 1,650.00CNY

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889453-78-5SDS

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 4-Methoxyphenyl 3-O-Allyl-2-azido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names (3)-(+)-3-(Boc-amino)pyrrolidine

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:889453-78-5 SDS

889453-78-5Downstream Products

889453-78-5Relevant articles and documents

Straightforward sequential and one-pot synthesis of a pentasaccharide repeating unit corresponding to the cell wall O-antigen of Shigella boydii type 18

Shit, Pradip,Gucchait, Arin,Misra, Anup Kumar

, (2019)

Synthesis of a pentasaccharide repeating unit corresponding to the cell of wall O-antigen Shigella boydii type 18 has been achieved by sequential as well as iterative glycosylations in one-pot. Use of p-methoxybenzyl group (PMB) as an in situ removable pr

Concise synthesis of a tetrasaccharide related to the repeating unit of the cell wall O-antigen of Salmonella enterica O60

Gucchait, Arin,Misra, Anup Kumar,Shit, Pradip

, (2020/07/25)

Synthesis of a tetrasaccharide related to the repeating unit of the cell wall O-antigen of Salmonella enterica O60 has been achieved by sequential glycosylations in very good yield. Use of p-methoxybenzyl group (PMB) as an in situ removable protecting gro

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