Cas 240415-64-9,tert-Butoxycarbonylamino-acetic acid (3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-yl ester

240415-64-9

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Basic information

Product Name: tert-Butoxycarbonylamino-acetic acid (3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-yl ester
Synonyms: tert-Butoxycarbonylamino-acetic acid (3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-yl ester
CAS NO:240415-64-9
Molecular Formula:
Molecular Weight: 603.712
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: tert-Butoxycarbonylamino-acetic acid (3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: tert-Butoxycarbonylamino-acetic acid (3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-yl ester(240415-64-9)
EPA Substance Registry System: tert-Butoxycarbonylamino-acetic acid (3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-yl ester(240415-64-9)

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: 240415-64-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 240415-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,4,1 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 240415-64:
(8*2)+(7*4)+(6*0)+(5*4)+(4*1)+(3*5)+(2*6)+(1*4)=99
99 % 10 = 9
So 240415-64-9 is a valid CAS Registry Number.

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240415-64-9Relevant academic research and scientific papers

Claisen-Ireland rearrangement: A new route to C-glycosides

Vidal, Thierry,Haudrechy, Arnaud,Langlois, Yves

, p. 5677 - 5680 (2007/10/03)

A Claisen-Ireland rearrangement led to the formation of C-glycan derivatives. Azidonitration-reduction or dihydroxylation afforded gluco- and galacto-derived β-C-glycosides. Subsequent deprotonation of bicyclic lactones 16 allowed the control of the newly created asymmetric centre.

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