Cas 224184-72-9,2-(3,4,6-tri-O-acetyl-2-bromo-2-deoxy-β-D-gluco-pyranosyl)-thio-2-thiono-5,5-dimethyl-1,3,2-dioxaphosphorinane

224184-72-9

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Basic information

Product Name: 2-(3,4,6-tri-O-acetyl-2-bromo-2-deoxy-β-D-gluco-pyranosyl)-thio-2-thiono-5,5-dimethyl-1,3,2-dioxaphosphorinane
Synonyms: 2-(3,4,6-tri-O-acetyl-2-bromo-2-deoxy-β-D-gluco-pyranosyl)-thio-2-thiono-5,5-dimethyl-1,3,2-dioxaphosphorinane
CAS NO:224184-72-9
Molecular Formula:
Molecular Weight: 549.398
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-(3,4,6-tri-O-acetyl-2-bromo-2-deoxy-β-D-gluco-pyranosyl)-thio-2-thiono-5,5-dimethyl-1,3,2-dioxaphosphorinane(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3,4,6-tri-O-acetyl-2-bromo-2-deoxy-β-D-gluco-pyranosyl)-thio-2-thiono-5,5-dimethyl-1,3,2-dioxaphosphorinane(224184-72-9)
EPA Substance Registry System: 2-(3,4,6-tri-O-acetyl-2-bromo-2-deoxy-β-D-gluco-pyranosyl)-thio-2-thiono-5,5-dimethyl-1,3,2-dioxaphosphorinane(224184-72-9)

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: 224184-72-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 224184-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,4,1,8 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 224184-72:
(8*2)+(7*2)+(6*4)+(5*1)+(4*8)+(3*4)+(2*7)+(1*2)=119
119 % 10 = 9
So 224184-72-9 is a valid CAS Registry Number.

224184-72-9Upstream product

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224184-72-9Relevant academic research and scientific papers

New derivatives of α-and β-dithiophosphates of 2-bromo-2-deoxy sugars

Borowiecka

, p. 793 - 798 (2007/10/03)

New derivatives of 2-bromo-2-deoxy hexopyranose, α-and β-glycosyl dithiophosphates 6-11, were synthesized by three methods: (A) by glycosylation of alkyl salts 1-3 of phosphorodithio acids with α-1,2-D-gluco and α-1-2-D-manno dibromides 4, 5; (B) by reaction of 4 or 5 with free phosphorodithio acids 12-14 activated by Lewis acid; (C) by addition of dithioacids 12-14 to 2-bromo-D-glucal 15.

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