Cas 80779-88-0,(2-O-acetyl-3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-2-O-acetyl-3,4,6-tetra-O-benzyl-β-D-mannopyranoside

80779-88-0

Post Buying Request

Basic information

Product Name: (2-O-acetyl-3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-2-O-acetyl-3,4,6-tetra-O-benzyl-β-D-mannopyranoside
Synonyms:
CAS NO:80779-88-0
Molecular Formula:
Molecular Weight: 967.122
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2-O-acetyl-3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-2-O-acetyl-3,4,6-tetra-O-benzyl-β-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: (2-O-acetyl-3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-2-O-acetyl-3,4,6-tetra-O-benzyl-β-D-mannopyranoside(80779-88-0)
EPA Substance Registry System: (2-O-acetyl-3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-2-O-acetyl-3,4,6-tetra-O-benzyl-β-D-mannopyranoside(80779-88-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 80779-88-0(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

80779-88-0 Suppliers

Recommended suppliers

80779-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80779-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,7 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80779-88:
(7*8)+(6*0)+(5*7)+(4*7)+(3*9)+(2*8)+(1*8)=170
170 % 10 = 0
So 80779-88-0 is a valid CAS Registry Number.

80779-88-0Upstream product

324041-25-0 3,4,6-tri-O-benzoyl-1,2-O-[(RS)-1-methoxyethane-1,1-diyl]-β-D-mannopyranose

80779-88-0Downstream Products

80779-88-0Relevant academic research and scientific papers

Unexpected stereocontrolled access to 1α,1′β-disaccharides from methyl 1,2-ortho esters

Uriel, Clara,Ventura, Juan,Gomez, Ana M.,Lopez, J. Cristobal,Fraser-Reid, Bert

, p. 795 - 800 (2012)

Mannopyranose-derived methyl 1,2-orthoacetates (R = Me) and 1,2-orthobenzoates (R = Ph) undergo stereoselective formation of 1α,1′β-disaccharides, upon treatment with BF 3?Et2O in CH2Cl2, rather than the expected acid-catalyzed reaction leading to methyl glycosides by way of a rearrangement-glycosylation process of the liberated methanol.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 80779-88-0