Cas 1055313-16-0,allenyl 2,3-dideoxy-4-O-t-butyldimethylsilyl-6-O-triphenylmethyl-α-D-glucopyranoside

1055313-16-0

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Basic information

Product Name: allenyl 2,3-dideoxy-4-O-t-butyldimethylsilyl-6-O-triphenylmethyl-α-D-glucopyranoside
Synonyms:
CAS NO:1055313-16-0
Molecular Formula:
Molecular Weight: 542.791
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: allenyl 2,3-dideoxy-4-O-t-butyldimethylsilyl-6-O-triphenylmethyl-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: allenyl 2,3-dideoxy-4-O-t-butyldimethylsilyl-6-O-triphenylmethyl-α-D-glucopyranoside(1055313-16-0)
EPA Substance Registry System: allenyl 2,3-dideoxy-4-O-t-butyldimethylsilyl-6-O-triphenylmethyl-α-D-glucopyranoside(1055313-16-0)

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: 1055313-16-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1055313-16-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,5,3,1 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1055313-16:
(9*1)+(8*0)+(7*5)+(6*5)+(5*3)+(4*1)+(3*3)+(2*1)+(1*6)=110
110 % 10 = 0
So 1055313-16-0 is a valid CAS Registry Number.

1055313-16-0Upstream product

1055313-14-8 propargyl 2,3-dideoxy-4-O-t-butyldimethylsilyl-6-O-triphenylmethyl-α-D-glucopyranoside

1055313-16-0Downstream Products

1055313-16-0Relevant academic research and scientific papers

Traceless chiral auxiliaries for the allene ether Nazarov cyclization

Banaag, April R.,Tius, Marcus A.

supporting information; experimental part, p. 8133 - 8141 (2009/04/04)

(Chemical Equation Presented) The key stereochemical factors that determine transfer of asymmetry from the chiral auxiliary to the cyclopentenone in the allene ether version of the Nazarov reaction have been elucidated. On the basis of the new insights in

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