Cas 163593-01-9,1-N,N-dimethylsulfamoyl-2-tert-butyldimethylsilyl-5-(5-O-trityl-2-deoxy-D-erythro-pent-1-enofuranosyl)-1H-imidazole

163593-01-9

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Basic information

Product Name: 1-N,N-dimethylsulfamoyl-2-tert-butyldimethylsilyl-5-(5-O-trityl-2-deoxy-D-erythro-pent-1-enofuranosyl)-1H-imidazole
Synonyms: 1-N,N-dimethylsulfamoyl-2-tert-butyldimethylsilyl-5-(5-O-trityl-2-deoxy-D-erythro-pent-1-enofuranosyl)-1H-imidazole
CAS NO:163593-01-9
Molecular Formula:
Molecular Weight: 645.895
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: 1-N,N-dimethylsulfamoyl-2-tert-butyldimethylsilyl-5-(5-O-trityl-2-deoxy-D-erythro-pent-1-enofuranosyl)-1H-imidazole(CAS DataBase Reference)
NIST Chemistry Reference: 1-N,N-dimethylsulfamoyl-2-tert-butyldimethylsilyl-5-(5-O-trityl-2-deoxy-D-erythro-pent-1-enofuranosyl)-1H-imidazole(163593-01-9)
EPA Substance Registry System: 1-N,N-dimethylsulfamoyl-2-tert-butyldimethylsilyl-5-(5-O-trityl-2-deoxy-D-erythro-pent-1-enofuranosyl)-1H-imidazole(163593-01-9)

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: 163593-01-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 163593-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,5,9 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 163593-01:
(8*1)+(7*6)+(6*3)+(5*5)+(4*9)+(3*3)+(2*0)+(1*1)=139
139 % 10 = 9
So 163593-01-9 is a valid CAS Registry Number.

163593-01-9Upstream product

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163593-01-9Relevant academic research and scientific papers

New route to 1-(5-imidazolyl)ribofuranoid glycals from ribofuranosyl chloride and 5-lithio-imidazole

Harusawa,Kawabata,Murai,Yoneda,Kurihara

, p. 152 - 155 (1995)

Reaction of ribofuranosyl chlorides with 2 eq of 5-lithio-imidazole afforded 1-(5-imidazolyl)ribofuranoid glycals in good yields. Hydrolysis of the glycal (3) with hydrochloric acid led to 4-(5-hydroxymethylfuran-2-yl)imidazole (7), which contains both hy

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