Cas 384371-53-3,Allyl 2D,3D,5D-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-[2C,3C,4C,6C-tetra-O-acetyl-β-D-glucopyranosyl-(1->3)]-2B-O-benzoyl-α-L-rhamnopyranoside

384371-53-3

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Basic information

Product Name: Allyl 2^D,3^D,5^D-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-[2^C,3^C,4^C,6^C-tetra-O-acetyl-β-D-glucopyranosyl-(1->3)]-2^B-O-benzoyl-α-L-rhamnopyranoside
Synonyms: Allyl 2^D,3^D,5^D-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-[2^C,3^C,4^C,6^C-tetra-O-acetyl-β-D-glucopyranosyl-(1->3)]-2^B-O-benzoyl-α-L-rhamnopyranoside
CAS NO:384371-53-3
Molecular Formula:
Molecular Weight: 1083.06
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: Allyl 2^D,3^D,5^D-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-[2^C,3^C,4^C,6^C-tetra-O-acetyl-β-D-glucopyranosyl-(1->3)]-2^B-O-benzoyl-α-L-rhamnopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: Allyl 2^D,3^D,5^D-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-[2^C,3^C,4^C,6^C-tetra-O-acetyl-β-D-glucopyranosyl-(1->3)]-2^B-O-benzoyl-α-L-rhamnopyranoside(384371-53-3)
EPA Substance Registry System: Allyl 2^D,3^D,5^D-tri-O-benzoyl-α-L-arabinofuranosyl-(1->4)-[2^C,3^C,4^C,6^C-tetra-O-acetyl-β-D-glucopyranosyl-(1->3)]-2^B-O-benzoyl-α-L-rhamnopyranoside(384371-53-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 384371-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 384371-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,4,3,7 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 384371-53:
(8*3)+(7*8)+(6*4)+(5*3)+(4*7)+(3*1)+(2*5)+(1*3)=163
163 % 10 = 3
So 384371-53-3 is a valid CAS Registry Number.

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384371-53-3Relevant academic research and scientific papers

An effcient synthesis of julibrosides related to neosaponin

Du,Zhang,Kong

, p. 2289 - 2293 (2007/10/03)

A practical method is developed for the synthesis of neosaponin cholest-5(6)-en-3β-yl β-D-glucopyranosyl-(1→3)-[α-L-arabinofuranosyl-(1→4)]- α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside. This julibroside mimic shows cytotoxic activity towards P388 (mouse leukaemia) with GI50 = 22.5 μg mL-1.

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