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[(R)-3-(Acetylhydroxyamino)-2-hydroxypropyl]phosphonic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73240-15-0

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73240-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73240-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,4 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73240-15:
(7*7)+(6*3)+(5*2)+(4*4)+(3*0)+(2*1)+(1*5)=100
100 % 10 = 0
So 73240-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H12NO6P/c1-4(7)6(9)2-5(8)3-13(10,11)12/h5,8-9H,2-3H2,1H3,(H2,10,11,12)/t5-/m1/s1

73240-15-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R)-3-[acetyl(hydroxy)amino]-2-hydroxypropyl]phosphonic acid

1.2 Other means of identification

Product number -
Other names Phosphonic acid,(3-(acetylhydroxyamino)-2-hydroxypropyl)-,(R)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73240-15-0 SDS

73240-15-0Downstream Products

73240-15-0Relevant academic research and scientific papers

Characterization and application of the Fe(ii) and α-ketoglutarate dependent hydroxylase FrbJ

Desieno, Matthew A.,Van Der Donk, Wilfred A.,Zhao, Huimin

, p. 10025 - 10027 (2011)

The Fe(ii) and α-ketoglutarate-dependent hydroxylase FrbJ was previously demonstrated to utilize FR-900098 synthesizing a second phosphonate FR-33289. Here we assessed its ability to hydroxylate other possible substrates, generating a library of potential antimalarial compounds. Through a series of bioassays and in vitro experiments, we identified two new antimalarials. The Royal Society of Chemistry 2011.

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