Cas 685850-69-5,2-benzylthio-4,5-dihydro-(3',5'-di-O-tert-butyldimethylsilyl-1',2'-dideoxy-β-D-xylofuranoso)[1,2-d]-oxazole

685850-69-5

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Basic information

Product Name: 2-benzylthio-4,5-dihydro-(3',5'-di-O-tert-butyldimethylsilyl-1',2'-dideoxy-β-D-xylofuranoso)[1,2-d]-oxazole
Synonyms:
CAS NO:685850-69-5
Molecular Formula:
Molecular Weight: 509.858
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: 2-benzylthio-4,5-dihydro-(3',5'-di-O-tert-butyldimethylsilyl-1',2'-dideoxy-β-D-xylofuranoso)[1,2-d]-oxazole(CAS DataBase Reference)
NIST Chemistry Reference: 2-benzylthio-4,5-dihydro-(3',5'-di-O-tert-butyldimethylsilyl-1',2'-dideoxy-β-D-xylofuranoso)[1,2-d]-oxazole(685850-69-5)
EPA Substance Registry System: 2-benzylthio-4,5-dihydro-(3',5'-di-O-tert-butyldimethylsilyl-1',2'-dideoxy-β-D-xylofuranoso)[1,2-d]-oxazole(685850-69-5)

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: 685850-69-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 685850-69-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,8,5 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 685850-69:
(8*6)+(7*8)+(6*5)+(5*8)+(4*5)+(3*0)+(2*6)+(1*9)=215
215 % 10 = 5
So 685850-69-5 is a valid CAS Registry Number.

685850-69-5Upstream product

685850-69-5Downstream Products

685850-69-5Relevant academic research and scientific papers

Small libraries of fused quinazolinone-sugars. Access to quinazolinedione nucleosides

Girniene, Jolanta,Apremont, Guillaume,Tatibou?t, Arnaud,Sackus, Algirdas,Rollin, Patrick

, p. 2609 - 2619 (2004)

Unprotected carbohydrates can readily be converted into base-modified nucleosides and deoxynucleosides through a short sequence involving the condensation of anthranilic acid derivatives with a suitably protected sugar-derived 2-alkylthio-1,3-oxazoline.

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