Cas 905711-08-2,(2S,3R)-1-tert-butyldiphenylsilyloxy-3-tert-butoxycarbonylamino-2-(p-nitrobenzoyloxy)-5-hexene

905711-08-2

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Basic information

Product Name: (2S,3R)-1-tert-butyldiphenylsilyloxy-3-tert-butoxycarbonylamino-2-(p-nitrobenzoyloxy)-5-hexene
Synonyms: (2S,3R)-1-tert-butyldiphenylsilyloxy-3-tert-butoxycarbonylamino-2-(p-nitrobenzoyloxy)-5-hexene
CAS NO:905711-08-2
Molecular Formula:
Molecular Weight: 618.802
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: (2S,3R)-1-tert-butyldiphenylsilyloxy-3-tert-butoxycarbonylamino-2-(p-nitrobenzoyloxy)-5-hexene(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R)-1-tert-butyldiphenylsilyloxy-3-tert-butoxycarbonylamino-2-(p-nitrobenzoyloxy)-5-hexene(905711-08-2)
EPA Substance Registry System: (2S,3R)-1-tert-butyldiphenylsilyloxy-3-tert-butoxycarbonylamino-2-(p-nitrobenzoyloxy)-5-hexene(905711-08-2)

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: 905711-08-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 905711-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,7,1 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 905711-08:
(8*9)+(7*0)+(6*5)+(5*7)+(4*1)+(3*1)+(2*0)+(1*8)=152
152 % 10 = 2
So 905711-08-2 is a valid CAS Registry Number.

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905711-08-2Downstream Products

905711-08-2Relevant academic research and scientific papers

Stereodivergent syntheses of conduramines and aminocyclitols

Alegret, Carlos,Benet-Buchholz, Jordi,Riera, Antoni

, p. 3069 - 3072 (2006)

The diastereomers of 6-amino-cyclohex-3-ene-1,2-diols 1 (4-deoxy-3-conduramines), key building blocks for the syntheses of a large range of natural products, have been enantioselectively prepared. Diastereoselective dihydroxylation of the compounds provid

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