Cas 126004-12-4,benzyl N-tert-butoxycarbonyl-2-amino-6-diethoxyphosphonate-6-thio-(2'-pyridyl)-L-pimelic ester

126004-12-4

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Basic information

Product Name: benzyl N-tert-butoxycarbonyl-2-amino-6-diethoxyphosphonate-6-thio-(2'-pyridyl)-L-pimelic ester
Synonyms: benzyl N-tert-butoxycarbonyl-2-amino-6-diethoxyphosphonate-6-thio-(2'-pyridyl)-L-pimelic ester
CAS NO:126004-12-4
Molecular Formula:
Molecular Weight: 566.656
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: benzyl N-tert-butoxycarbonyl-2-amino-6-diethoxyphosphonate-6-thio-(2'-pyridyl)-L-pimelic ester(CAS DataBase Reference)
NIST Chemistry Reference: benzyl N-tert-butoxycarbonyl-2-amino-6-diethoxyphosphonate-6-thio-(2'-pyridyl)-L-pimelic ester(126004-12-4)
EPA Substance Registry System: benzyl N-tert-butoxycarbonyl-2-amino-6-diethoxyphosphonate-6-thio-(2'-pyridyl)-L-pimelic ester(126004-12-4)

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: 126004-12-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126004-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,0 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126004-12:
(8*1)+(7*2)+(6*6)+(5*0)+(4*0)+(3*4)+(2*1)+(1*2)=74
74 % 10 = 4
So 126004-12-4 is a valid CAS Registry Number.

126004-12-4Upstream product

30924-93-7 α-benzyl N^α-(tert-butyloxycarbonyl)-L-glutamate

126004-12-4Downstream Products

125982-82-3 benzyl N-tert-butoxycarbonyl-2-amino-6-diethoxyphosphonate-L-caproic ester

126004-12-4Relevant academic research and scientific papers

New synthesis of sugar, nucleoside and α-amino acid phosphonates

Barton,Gero,Quiclet-Sire,Samadi

, p. 1627 - 1636 (1992)

Photolysis of N-hydroxy-2-thiopyridone esters derived from uronic acids of α-amino acids in presence of vinyl phosphonate affords the corresponding phosphonate derivatives. A convenient route for the synthesis of the isostere of AZT-5' monophosphate is de

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