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CAS

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343783-04-0

diethyl (ethyl, 2-O-benzylhydroxylamino) phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 343783-04-0 Structure

  • Basic information

    1. Product Name: diethyl (ethyl, 2-O-benzylhydroxylamino) phosphonate
    2. Synonyms: diethyl (ethyl, 2-O-benzylhydroxylamino) phosphonate
    3. CAS NO:343783-04-0
    4. Molecular Formula:
    5. Molecular Weight: 287.296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 343783-04-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: diethyl (ethyl, 2-O-benzylhydroxylamino) phosphonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl (ethyl, 2-O-benzylhydroxylamino) phosphonate(343783-04-0)
    11. EPA Substance Registry System: diethyl (ethyl, 2-O-benzylhydroxylamino) phosphonate(343783-04-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 343783-04-0(Hazardous Substances Data)

343783-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 343783-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,7,8 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 343783-04:
(8*3)+(7*4)+(6*3)+(5*7)+(4*8)+(3*3)+(2*0)+(1*4)=150
150 % 10 = 0
So 343783-04-0 is a valid CAS Registry Number.

343783-04-0Downstream Products

343783-04-0Relevant articles and documents

The effect of chain length and unsaturation on Mtb Dxr inhibition and antitubercular killing activity of FR900098 analogs

Jackson, Emily R.,San Jose, Géraldine,Brothers, Robert C.,Edelstein, Emma K.,Sheldon, Zachary,Haymond, Amanda,Johny, Chinchu,Boshoff, Helena I.,Couch, Robin D.,Dowd, Cynthia S.

, p. 649 - 653 (2014)

Inhibition of the nonmevalonate pathway (NMP) of isoprene biosynthesis has been examined as a source of new antibiotics with novel mechanisms of action. Dxr is the best studied of the NMP enzymes and several reports have described potent Dxr inhibitors. M

Selective inhibition of Trypanosoma brucei GAPDH by 1,3-bisphospho-D-glyceric acid (1,3-diPG) analogues

Ladame, Sylvain,Bardet, Michel,Périé, Jacques,Willson, Michèle

, p. 773 - 783 (2007/10/03)

Various phosphono-phosphates and diphophonates were synthesized as 1,3-diphosphoglycerate 1,3-diPG) analogues by using a β-ketophosphonate, an α-fluoro,β-ketophosphonate or a β-ketophosphoramidate to mimic the unstable carboxyphosphate part of the natural

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