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CAS

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148932-53-0

<4-(4-methoxyphenylsulfonamido)butylcarbamoylmethyl>-1,4,7,10-tetraazacyclododecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148932-53-0 Structure

  • Basic information

    1. Product Name: <4-(4-methoxyphenylsulfonamido)butylcarbamoylmethyl>-1,4,7,10-tetraazacyclododecane
    2. Synonyms: <4-(4-methoxyphenylsulfonamido)butylcarbamoylmethyl>-1,4,7,10-tetraazacyclododecane
    3. CAS NO:148932-53-0
    4. Molecular Formula:
    5. Molecular Weight: 470.637
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148932-53-0.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: <4-(4-methoxyphenylsulfonamido)butylcarbamoylmethyl>-1,4,7,10-tetraazacyclododecane(CAS DataBase Reference)
    10. NIST Chemistry Reference: <4-(4-methoxyphenylsulfonamido)butylcarbamoylmethyl>-1,4,7,10-tetraazacyclododecane(148932-53-0)
    11. EPA Substance Registry System: <4-(4-methoxyphenylsulfonamido)butylcarbamoylmethyl>-1,4,7,10-tetraazacyclododecane(148932-53-0)

  • 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: 148932-53-0(Hazardous Substances Data)

148932-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148932-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,9,3 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 148932-53:
(8*1)+(7*4)+(6*8)+(5*9)+(4*3)+(3*2)+(2*5)+(1*3)=160
160 % 10 = 0
So 148932-53-0 is a valid CAS Registry Number.

148932-53-0Relevant articles and documents

Stable Anionic, Neutral and Cationic Complexes of Gadolinium with Functionalised Amino-phosphinic Acid Macrocyclic Ligands

Parker, David,Pulukkody, Kanthi,Norman, Timothy J.,Harrison, Alice,Royle, Louise,Walker, Carol

, p. 1441 - 1443 (1992)

The synthesis and stability of anionic, neutral and cationic gadolinium complexes based on tetraazaphosphinic acid ligands is compared: lipophilic anionic complexes show biliary rather than renal clearance.

Synthesis of Charged and Uncharged Complexes of Gadolinium and Yttrium with Cyclic Polyazaphosphinic Acid Ligands for in vivo Applications

Pulukkody, Kanthi P.,Norman, Timothy J.,Parker, David,Royle, Louise,Broan, Christopher J.

, p. 605 - 620 (2007/10/02)

The synthesis of 18 new macrocyclic complexing agents incorporating phosphinic acid (and carboxylic acid) groups is reported, based on the 1,4,7,10-tetraazacyclododecane ring.Through selective functionalisation of one ring nitrogen or by changing the natu

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