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Methyl 2-O-Allyl-3-O-(2',3',4',6'-tetra-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside, with the CAS number 81555-75-1, is a complex organic compound that plays a significant role in the field of organic synthesis. It is characterized by its unique structure, which includes a methyl group, allyl group, and a tetra-O-acetyl-α-D-mannopyranosyl moiety attached to an α-D-mannopyranoside backbone. This intricate arrangement of functional groups makes it a versatile building block for the synthesis of various organic molecules.

81555-75-1

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81555-75-1 Usage

Uses

Used in Organic Synthesis:
Methyl 2-O-Allyl-3-O-(2',3',4',6'-tetra-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside is used as a key intermediate in organic synthesis for the preparation of a wide range of compounds. Its unique structure allows for the formation of various derivatives through chemical reactions, making it a valuable component in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Methyl 2-O-Allyl-3-O-(2',3',4',6'-tetra-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside is used as a building block for the development of novel drug candidates. Its ability to form diverse derivatives through organic synthesis makes it a promising starting material for the creation of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
Methyl 2-O-Allyl-3-O-(2',3',4',6'-tetra-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside also finds application in the agrochemical industry, where it serves as a precursor for the synthesis of new agrochemicals. Its unique structure can be utilized to develop innovative compounds with improved efficacy and selectivity in crop protection and other agricultural applications.
Used in Specialty Chemicals:
In the specialty chemicals sector, Methyl 2-O-Allyl-3-O-(2',3',4',6'-tetra-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside is employed as a versatile intermediate for the synthesis of various specialty chemicals. Its potential applications include the development of new materials with unique properties, such as advanced polymers, surfactants, and other high-value chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 81555-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,5 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81555-75:
(7*8)+(6*1)+(5*5)+(4*5)+(3*5)+(2*7)+(1*5)=141
141 % 10 = 1
So 81555-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H36O15/c1-7-8-32-21-19(17(30)15(9-25)37-23(21)31-6)39-24-22(36-14(5)29)20(35-13(4)28)18(34-12(3)27)16(38-24)10-33-11(2)26/h7,15-25,30H,1,8-10H2,2-6H3

81555-75-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-O-allyl-3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-α-D-mannopyranoside

1.2 Other means of identification

Product number -
Other names (2R,3S,4R,5R,6S)-5-Hydroxy-2-methoxy-6-methyl-4-(tosyloxy)tetrahydro-2H-pyran-3-yl acetate

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:81555-75-1 SDS

81555-75-1Relevant academic research and scientific papers

Syntheses of model oligosaccharides of biological significance. Synthesis of methyl 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-d-mannopyranoside and the corresponding mannobiosides.

Winnik,Brisson,Carver,Krepinsky

, p. 15 - 28 (2007/10/02)

Methyl 2-O-allyl-4,6-O-benzylidene-3-O-(2,3,4,6-tetra-O-acetyl-alpha-D-mannopyranosyl) -alpha-D-mannopyranoside (12) was prepared in 90% yield by Helferich glycosylation of methyl 2-O-allyl-4,6-O-benzylidene-alpha-D-mannopyranoside (9) with tetra-O-acetyl

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