Cas 1374431-75-0,methyl O-(3,4,6-tri-O-acetyl-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

1374431-75-0

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Basic information

Product Name: methyl O-(3,4,6-tri-O-acetyl-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside
Synonyms:
CAS NO:1374431-75-0
Molecular Formula:
Molecular Weight: 897.2
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: methyl O-(3,4,6-tri-O-acetyl-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl O-(3,4,6-tri-O-acetyl-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside(1374431-75-0)
EPA Substance Registry System: methyl O-(3,4,6-tri-O-acetyl-2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside(1374431-75-0)

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: 1374431-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1374431-75-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,4,3 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1374431-75:
(9*1)+(8*3)+(7*7)+(6*4)+(5*4)+(4*3)+(3*1)+(2*7)+(1*5)=160
160 % 10 = 0
So 1374431-75-0 is a valid CAS Registry Number.

1374431-75-0Upstream product

53008-65-4 methyl 2,3,4-tri-O-benzyl-D-glucopyranoside

1374431-75-0Downstream Products

1374431-75-0Relevant academic research and scientific papers

Highly selective formation of β-glycosides of N-acetylglucosamine using catalytic iron(III) Triflate

Stevenin, Arnaud,Boyer, Francois-Didier,Beau, Jean-Marie

, p. 1699 - 1702 (2012)

Efficient and highly selective glycosylation reactions of peracetylated β-D-N-acetylglucosamine are described using catalytic iron(III) triflate and 2,4,6-tri-tert-butylpyrimidine (TTBP) under microwave conditions. We have demonstrated that the formation of β-(1→6) and β-(1→3) linked disaccharides are obtained in high yields in the presence ofvarious protecting groups.

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