Cas 878675-41-3,[(S)-1-((2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-hexadecyloxymethyl-tetrahydro-furan-2-ylmethyl)-pyrrolidin-2-yl]-methanol

878675-41-3

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Basic information

Product Name: [(S)-1-((2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-hexadecyloxymethyl-tetrahydro-furan-2-ylmethyl)-pyrrolidin-2-yl]-methanol
Synonyms:
CAS NO:878675-41-3
Molecular Formula:
Molecular Weight: 651.971
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: [(S)-1-((2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-hexadecyloxymethyl-tetrahydro-furan-2-ylmethyl)-pyrrolidin-2-yl]-methanol(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-1-((2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-hexadecyloxymethyl-tetrahydro-furan-2-ylmethyl)-pyrrolidin-2-yl]-methanol(878675-41-3)
EPA Substance Registry System: [(S)-1-((2R,3R,4R,5R)-3,4-Bis-benzyloxy-5-hexadecyloxymethyl-tetrahydro-furan-2-ylmethyl)-pyrrolidin-2-yl]-methanol(878675-41-3)

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: 878675-41-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 878675-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,6,7 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 878675-41:
(8*8)+(7*7)+(6*8)+(5*6)+(4*7)+(3*5)+(2*4)+(1*1)=243
243 % 10 = 3
So 878675-41-3 is a valid CAS Registry Number.

878675-41-3Upstream product

878675-41-3Downstream Products

878675-41-3Relevant academic research and scientific papers

Hydrolytically stable arabinofuranoside analogs for the synthesis of arabinosyltransferase inhibitors

Chaumontet, Manon,Pons, Valérie,Marotte, Karine,Prandi, Jacques

, p. 1113 - 1116 (2007/10/03)

The first members of two new families of arabinosyltransferase inhibitors, derived from previously reported hybrid compounds covalently associating an iminoalditol with an α-d-arabinofuranoside, have been prepared. In place of the arabinofuranoside moiety

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