Cas 884856-12-6,(2-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucpyranosyl) dibenzyl phosphate

884856-12-6

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Basic information

Product Name: (2-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucpyranosyl) dibenzyl phosphate
Synonyms:
CAS NO:884856-12-6
Molecular Formula:
Molecular Weight: 735.774
EINECS: N/A
Product Categories: N/A
Mol File: 884856-12-6.mol
Article Data: 1

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-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucpyranosyl) dibenzyl phosphate(CAS DataBase Reference)
NIST Chemistry Reference: (2-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucpyranosyl) dibenzyl phosphate(884856-12-6)
EPA Substance Registry System: (2-azido-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucpyranosyl) dibenzyl phosphate(884856-12-6)

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: 884856-12-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 884856-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,8,5 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 884856-12:
(8*8)+(7*8)+(6*4)+(5*8)+(4*5)+(3*6)+(2*1)+(1*2)=226
226 % 10 = 6
So 884856-12-6 is a valid CAS Registry Number.

884856-12-6Upstream product

108549-23-1 Dibenzyl N,N-diisopropylphosphoramidite

884856-12-6Downstream Products

2152-75-2 2-amino-2-deoxy-D-glucopyranose-1-(dihydrogen phosphate)

884856-12-6Relevant articles and documents

Artificial N-functionalized UDP-glucosamine analogues as modified substrates for N-acetylglucosaminyl transferases

Lazarevic, Daniel,Thiem, Joachim

, p. 569 - 576 (2006)

Analogues of UDP-GlcNAc modified at the 2-acetamido group of the GlcNAc moiety were prepared in order to study their role in the mechanism of N-acetylglucosaminyl transferase mediated glycosylation reactions. The structural analogues with N-formyl-, N-pro

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