Cas 1152421-42-5,benzyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside

1152421-42-5

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Basic information

Product Name: benzyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside
Synonyms: benzyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside
CAS NO:1152421-42-5
Molecular Formula:
Molecular Weight: 1070.16
EINECS: N/A
Product Categories: N/A
Mol File: 1152421-42-5.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: benzyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside(1152421-42-5)
EPA Substance Registry System: benzyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside(1152421-42-5)

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: 1152421-42-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1152421-42-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,2,4,2 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1152421-42:
(9*1)+(8*1)+(7*5)+(6*2)+(5*4)+(4*2)+(3*1)+(2*4)+(1*2)=105
105 % 10 = 5
So 1152421-42-5 is a valid CAS Registry Number.

1152421-42-5Upstream product

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1152421-42-5Relevant articles and documents

Endo-β-N-acetylglucosaminidase-catalyzed polymerization of β-Glcp-(1→4)-GlcpNAc oxazoline: a revisit to enzymatic transglycosylation

Ochiai, Hirofumi,Huang, Wei,Wang, Lai-Xi

experimental part, p. 592 - 598 (2009/05/11)

An alternative synthesis of β-Glcp-(1→4)-GlcpNAc oxazoline is described, and its enzymatic reaction with the endo-β-N-acetylglucosaminidase from Arthrobacter protophormiae (Endo-A) was re-investigated. Under normal transglycosylation conditions with a cat

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