Cas 145389-73-7,(S)-3-(Dimethylphosphono)-2-((9-fluorenyl)methoxycarbamoyl)propionic acid

145389-73-7

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Basic information

Product Name: (S)-3-(Dimethylphosphono)-2-((9-fluorenyl)methoxycarbamoyl)propionic acid
Synonyms: (S)-3-(Dimethylphosphono)-2-((9-fluorenyl)methoxycarbamoyl)propionic acid
CAS NO:145389-73-7
Molecular Formula:
Molecular Weight: 419.371
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: (S)-3-(Dimethylphosphono)-2-((9-fluorenyl)methoxycarbamoyl)propionic acid(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-(Dimethylphosphono)-2-((9-fluorenyl)methoxycarbamoyl)propionic acid(145389-73-7)
EPA Substance Registry System: (S)-3-(Dimethylphosphono)-2-((9-fluorenyl)methoxycarbamoyl)propionic acid(145389-73-7)

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: 145389-73-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145389-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,3,8 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 145389-73:
(8*1)+(7*4)+(6*5)+(5*3)+(4*8)+(3*9)+(2*7)+(1*3)=157
157 % 10 = 7
So 145389-73-7 is a valid CAS Registry Number.

145389-73-7Upstream product

73724-45-5 N-(9H-fluoren-9-ylmethoxycarbonyl)-L-serine

145389-73-7Downstream Products

145389-73-7Relevant academic research and scientific papers

A Short Synthesis of (S)-3-(Dimethylphosphono)-2-((9-fluorenyl)methoxycarbamoyl)propionic Acid, a Protected Phosphonic Acid Analogue of Aspartic Acid

Hutchinson, Jonathan P. E.,Parkes, Kevin E. B.

, p. 7065 - 7066 (1992)

The synthesis, from serine, of a phosphonic acid analogue of aspartic acid protected in a form suitable for peptide synthesis, is described.

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