Cas 1244694-99-2,6-azidohexyl 2-O-(3-O-(2,4-di-O-benzyl-α-L-rhamnopyranosyl)-2,4-di-O-benzyl-α-L-rhamnopyranosyl)-3,4-di-O-benzyl-α-L-rhamnopyranoside

1244694-99-2

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Basic information

Product Name: 6-azidohexyl 2-O-(3-O-(2,4-di-O-benzyl-α-L-rhamnopyranosyl)-2,4-di-O-benzyl-α-L-rhamnopyranosyl)-3,4-di-O-benzyl-α-L-rhamnopyranoside
Synonyms:
CAS NO:1244694-99-2
Molecular Formula:
Molecular Weight: 1122.37
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-azidohexyl 2-O-(3-O-(2,4-di-O-benzyl-α-L-rhamnopyranosyl)-2,4-di-O-benzyl-α-L-rhamnopyranosyl)-3,4-di-O-benzyl-α-L-rhamnopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 6-azidohexyl 2-O-(3-O-(2,4-di-O-benzyl-α-L-rhamnopyranosyl)-2,4-di-O-benzyl-α-L-rhamnopyranosyl)-3,4-di-O-benzyl-α-L-rhamnopyranoside(1244694-99-2)
EPA Substance Registry System: 6-azidohexyl 2-O-(3-O-(2,4-di-O-benzyl-α-L-rhamnopyranosyl)-2,4-di-O-benzyl-α-L-rhamnopyranosyl)-3,4-di-O-benzyl-α-L-rhamnopyranoside(1244694-99-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1244694-99-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1244694-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,4,6,9 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1244694-99:
(9*1)+(8*2)+(7*4)+(6*4)+(5*6)+(4*9)+(3*4)+(2*9)+(1*9)=182
182 % 10 = 2
So 1244694-99-2 is a valid CAS Registry Number.

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1244694-99-2Relevant academic research and scientific papers

Combination of solid phase and solution phase synthesis of oligosaccharides using sonication

Tanifum, Christabel T.,Zhang, Jianjun,Chang, Cheng-Wei T.

scheme or table, p. 4323 - 4327 (2010/09/20)

An approach that combines solid phase and solution phase synthesis of oligosaccharides via the assistance of sonication has been developed. By employing the traceless linker, the designed oligosaccharides can be obtained in pure form and, more importantly

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