Cas 1433554-98-3,1-benzyloxycarbonylmethyl-1'-(2,3,4,6-tetra-O-acetyl-α-D-mannosyl)-4,4'-methylenebis(1H-1,2,3-triazole)

1433554-98-3

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Basic information

Product Name: 1-benzyloxycarbonylmethyl-1'-(2,3,4,6-tetra-O-acetyl-α-D-mannosyl)-4,4'-methylenebis(1H-1,2,3-triazole)
Synonyms: 1-benzyloxycarbonylmethyl-1'-(2,3,4,6-tetra-O-acetyl-α-D-mannosyl)-4,4'-methylenebis(1H-1,2,3-triazole)
CAS NO:1433554-98-3
Molecular Formula:
Molecular Weight: 628.596
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: 1-benzyloxycarbonylmethyl-1'-(2,3,4,6-tetra-O-acetyl-α-D-mannosyl)-4,4'-methylenebis(1H-1,2,3-triazole)(CAS DataBase Reference)
NIST Chemistry Reference: 1-benzyloxycarbonylmethyl-1'-(2,3,4,6-tetra-O-acetyl-α-D-mannosyl)-4,4'-methylenebis(1H-1,2,3-triazole)(1433554-98-3)
EPA Substance Registry System: 1-benzyloxycarbonylmethyl-1'-(2,3,4,6-tetra-O-acetyl-α-D-mannosyl)-4,4'-methylenebis(1H-1,2,3-triazole)(1433554-98-3)

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: 1433554-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1433554-98-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,3,5,5 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1433554-98:
(9*1)+(8*4)+(7*3)+(6*3)+(5*5)+(4*5)+(3*4)+(2*9)+(1*8)=163
163 % 10 = 3
So 1433554-98-3 is a valid CAS Registry Number.

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1433554-98-3Relevant academic research and scientific papers

Modulating lectin inhibition with N-glycosyl-1,2,3-triazole scaffolds

Azcune, Itxaso,Balentova, Eva,Sagartzazu-Aizpurua, Maialen,Ignacio Santos,Miranda, Jose I.,Fratila, Raluca M.,Aizpurua, Jesus M.

, p. 2434 - 2444 (2013/05/23)

The synthesis of three families of sialyl LewisX (sLe X) mimetics based on triazole and bis-triazole scaffolds is reported. The flexibility of these mimetics is dictated by the scaffold and gradually increases from flexible to rigid.

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