Cas 1292767-02-2,6,3',4',2'',5'',4'''-hexa-O-acetyl-1,3,2',6',2''',6'''-hexa-N-(tertbutoxycarbonyl)-5''-O-triphenylmethyl neomycin B

1292767-02-2

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Basic information

Product Name: 6,3',4',2'',5'',4'''-hexa-O-acetyl-1,3,2',6',2''',6'''-hexa-N-(tertbutoxycarbonyl)-5''-O-triphenylmethyl neomycin B
Synonyms: 6,3',4',2'',5'',4'''-hexa-O-acetyl-1,3,2',6',2''',6'''-hexa-N-(tertbutoxycarbonyl)-5''-O-triphenylmethyl neomycin B
CAS NO:1292767-02-2
Molecular Formula:
Molecular Weight: 1709.9
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: 6,3',4',2'',5'',4'''-hexa-O-acetyl-1,3,2',6',2''',6'''-hexa-N-(tertbutoxycarbonyl)-5''-O-triphenylmethyl neomycin B(CAS DataBase Reference)
NIST Chemistry Reference: 6,3',4',2'',5'',4'''-hexa-O-acetyl-1,3,2',6',2''',6'''-hexa-N-(tertbutoxycarbonyl)-5''-O-triphenylmethyl neomycin B(1292767-02-2)
EPA Substance Registry System: 6,3',4',2'',5'',4'''-hexa-O-acetyl-1,3,2',6',2''',6'''-hexa-N-(tertbutoxycarbonyl)-5''-O-triphenylmethyl neomycin B(1292767-02-2)

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: 1292767-02-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1292767-02-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,2,7,6 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1292767-02:
(9*1)+(8*2)+(7*9)+(6*2)+(5*7)+(4*6)+(3*7)+(2*0)+(1*2)=182
182 % 10 = 2
So 1292767-02-2 is a valid CAS Registry Number.

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1292767-02-2Relevant academic research and scientific papers

Synthesis and antibacterial activity of amphiphilic lysine-ligated neomycin B conjugates

Bera, Smritilekha,Zhanel, George G.,Schweizer, Frank

experimental part, p. 560 - 568 (2011/05/04)

Amphiphilic lysine-ligated neomycin B building blocks were prepared by reductive amination of a protected C5″-modified neomycin B-based aldehyde and side chain-unprotected lysine or lysine-containing peptides. It was demonstrated that a suitably protected

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