Cas 1049319-07-4,methyl 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-4-O-trifluoromethanesulfonyl-α-D-mannopyranoside

1049319-07-4

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Basic information

Product Name: methyl 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-4-O-trifluoromethanesulfonyl-α-D-mannopyranoside
Synonyms: methyl 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-4-O-trifluoromethanesulfonyl-α-D-mannopyranoside
CAS NO:1049319-07-4
Molecular Formula:
Molecular Weight: 545.493
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 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-4-O-trifluoromethanesulfonyl-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-4-O-trifluoromethanesulfonyl-α-D-mannopyranoside(1049319-07-4)
EPA Substance Registry System: methyl 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-4-O-trifluoromethanesulfonyl-α-D-mannopyranoside(1049319-07-4)

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: 1049319-07-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1049319-07-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,9,3,1 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1049319-07:
(9*1)+(8*0)+(7*4)+(6*9)+(5*3)+(4*1)+(3*9)+(2*0)+(1*7)=144
144 % 10 = 4
So 1049319-07-4 is a valid CAS Registry Number.

1049319-07-4Upstream product

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1049319-07-4Relevant academic research and scientific papers

Chemoenzymatic synthesis of CMP-N-acetyl-7-fluoro-7-deoxy-neuraminic acid

Hartlieb, Sina,Guenzel, Almut,Gerardy-Schahn, Rita,Muenster-Kuehnel, Anja K.,Kirschning, Andreas,Draeger, Gerald

, p. 2075 - 2082 (2008/12/21)

7-Fluoro sialic acid was prepared and activated as cytidine monophosphate (CMP) ester. The synthesis started with d-glucose, which was efficiently converted into N-acetyl-4-fluoro-4-deoxy-d-mannosamine. Aldolase catalyzed transformation yielded the corres

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