Cas 1007355-59-0,2,2-dimethyl-propionic acid [3-(acetyl-benzyloxy-amino)-butyl]-(2,2-dimethyl-propionyloxymethoxy)-phosphinoyloxymethyl ester

1007355-59-0

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Basic information

Product Name: 2,2-dimethyl-propionic acid [3-(acetyl-benzyloxy-amino)-butyl]-(2,2-dimethyl-propionyloxymethoxy)-phosphinoyloxymethyl ester
Synonyms:
CAS NO:1007355-59-0
Molecular Formula:
Molecular Weight: 529.568
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: 2,2-dimethyl-propionic acid [3-(acetyl-benzyloxy-amino)-butyl]-(2,2-dimethyl-propionyloxymethoxy)-phosphinoyloxymethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-dimethyl-propionic acid [3-(acetyl-benzyloxy-amino)-butyl]-(2,2-dimethyl-propionyloxymethoxy)-phosphinoyloxymethyl ester(1007355-59-0)
EPA Substance Registry System: 2,2-dimethyl-propionic acid [3-(acetyl-benzyloxy-amino)-butyl]-(2,2-dimethyl-propionyloxymethoxy)-phosphinoyloxymethyl ester(1007355-59-0)

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: 1007355-59-0(Hazardous Substances Data)

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1007355-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1007355-59-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,3,5 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1007355-59:
(9*1)+(8*0)+(7*0)+(6*7)+(5*3)+(4*5)+(3*5)+(2*5)+(1*9)=120
120 % 10 = 0
So 1007355-59-0 is a valid CAS Registry Number.

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1007355-59-0Relevant academic research and scientific papers

γ-substituted bis(pivaloyloxymethyl)ester analogues of fosmidomycin and FR900098

Kurz, Thomas,Behrendt, Christoph,Pein, Miriam,Kaula, Uwe,Bergmann, Baerbel,Walter, Rolf D.

, p. 661 - 666 (2007)

The synthesis and in-vitro antimalarial activity of γ-substituted bis(pivaloyloxymethyl)ester analogues of the drug candidate fosmidomycin have been investigated. In contrast to the high antimalarial activity of α-aryl substituted fosmidomycin analogues l

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