Cas 1193091-98-3,(E)-2-azido-2,4,5-trideoxy-1,3-bis-O-(4-methoxybenzyl)-6-O-undecyl-D-erythro-hex-4-enitol

1193091-98-3

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Basic information

Product Name: (E)-2-azido-2,4,5-trideoxy-1,3-bis-O-(4-methoxybenzyl)-6-O-undecyl-D-erythro-hex-4-enitol
Synonyms: (E)-2-azido-2,4,5-trideoxy-1,3-bis-O-(4-methoxybenzyl)-6-O-undecyl-D-erythro-hex-4-enitol
CAS NO:1193091-98-3
Molecular Formula:
Molecular Weight: 567.769
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: (E)-2-azido-2,4,5-trideoxy-1,3-bis-O-(4-methoxybenzyl)-6-O-undecyl-D-erythro-hex-4-enitol(CAS DataBase Reference)
NIST Chemistry Reference: (E)-2-azido-2,4,5-trideoxy-1,3-bis-O-(4-methoxybenzyl)-6-O-undecyl-D-erythro-hex-4-enitol(1193091-98-3)
EPA Substance Registry System: (E)-2-azido-2,4,5-trideoxy-1,3-bis-O-(4-methoxybenzyl)-6-O-undecyl-D-erythro-hex-4-enitol(1193091-98-3)

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: 1193091-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1193091-98-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,3,0,9 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1193091-98:
(9*1)+(8*1)+(7*9)+(6*3)+(5*0)+(4*9)+(3*1)+(2*9)+(1*8)=163
163 % 10 = 3
So 1193091-98-3 is a valid CAS Registry Number.

1193091-98-3Upstream product

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1193091-98-3Relevant academic research and scientific papers

Synthesis of 7-aza- and 7-thiasphingosines, and evaluation of their interaction with sphingosine kinases and with T-cells

Mathew, Thresen,Billaud, Celia,Billich, Andreas,Cavallari, Marco,Nussbaumer, Peter,De Libero, Gennaro,Vasella, Andrea

experimental part, p. 725 - 738 (2010/04/23)

The synthesis of 7-oxasphingosine (3) and 7-oxaceramide (4) was improved by starting from the 4-methoxybenzyl-protected d-galactal 9. The sphingosine analogues 5-7 and 24 were synthesized via the azido alcohol 13. The 7-thiasphingosine 5 is a poorer subst

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