Cas 151223-07-3,(R)-3-azido-1-O-benzyl-2-O-<(diisopropylphosphono)methyl>-1,2-propanediol

151223-07-3

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Basic information

Product Name: (R)-3-azido-1-O-benzyl-2-O-<(diisopropylphosphono)methyl>-1,2-propanediol
Synonyms: (R)-3-azido-1-O-benzyl-2-O-<(diisopropylphosphono)methyl>-1,2-propanediol
CAS NO:151223-07-3
Molecular Formula:
Molecular Weight: 385.4
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: (R)-3-azido-1-O-benzyl-2-O-<(diisopropylphosphono)methyl>-1,2-propanediol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-azido-1-O-benzyl-2-O-<(diisopropylphosphono)methyl>-1,2-propanediol(151223-07-3)
EPA Substance Registry System: (R)-3-azido-1-O-benzyl-2-O-<(diisopropylphosphono)methyl>-1,2-propanediol(151223-07-3)

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: 151223-07-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 151223-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,2,2 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 151223-07:
(8*1)+(7*5)+(6*1)+(5*2)+(4*2)+(3*3)+(2*0)+(1*7)=83
83 % 10 = 3
So 151223-07-3 is a valid CAS Registry Number.

151223-07-3Upstream product

151223-06-2 (S)-3-O-benzyl-2-O-<(diisopropylphosphono)methyl>-1-O-(methylsulfonyl)glycerol

151223-07-3Downstream Products

151223-07-3Relevant academic research and scientific papers

Synthesis and antiviral activity of 2'-substituted 9-[2- (phosphonomethoxy)ethyl]guanine analogues

Yu,Bronson,Yang,Patick,Alam,Brankovan,Datema,Hitchcock,Martin

, p. 2726 - 2738 (1993)

A series of 2'-substituted derivatives of 9-[2- (phosphonomethoxy)ethyl]guanine (PMEG, 1) have been synthesized and evaluated in vitro for anti-human immunodeficiency virus (HIV) activity in the XTT assay and for anti-herpes activity in the plaque reducti

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