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Decahydro-3soquinolineCarboxamideMonoBenzoate,NelfinavirMesylate, is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 201402-98-4 Structure
  • Basic information

    1. Product Name: Decahydro-3soquinolineCarboxamideMonoBenzoate,NelfinavirMesylate,
    2. Synonyms: 2-[3-Amino-2-Hydroxy-4-(Phenyl thio)-Butyl]-N-(1,1-dimethyl ethyl) Decahydro-3-isoquinoline Carboxamide Mono Benzoate;Decahydro- 3 –Isoquinoline Carboxamide Mono Benzoate, Nelfinavir Mesylate,;Decahydro-3soquinolineCarboxamideMonoBenzoate,NelfinavirMesylate,
    3. CAS NO:201402-98-4
    4. Molecular Formula: C31H45N3O4S
    5. Molecular Weight: 555.7717
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 201402-98-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Decahydro-3soquinolineCarboxamideMonoBenzoate,NelfinavirMesylate,(CAS DataBase Reference)
    10. NIST Chemistry Reference: Decahydro-3soquinolineCarboxamideMonoBenzoate,NelfinavirMesylate,(201402-98-4)
    11. EPA Substance Registry System: Decahydro-3soquinolineCarboxamideMonoBenzoate,NelfinavirMesylate,(201402-98-4)
  • 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: 201402-98-4(Hazardous Substances Data)

201402-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201402-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,4,0 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 201402-98:
(8*2)+(7*0)+(6*1)+(5*4)+(4*0)+(3*2)+(2*9)+(1*8)=74
74 % 10 = 4
So 201402-98-4 is a valid CAS Registry Number.

201402-98-4Downstream Products

201402-98-4Relevant articles and documents

Optimization of an electrolyte system for the simultaneous separation of nelfinavir mesylate and two impurities by micellar electrokinetic chromatography

Bastos, Carina A.,Gomes, Cláudia R. B.,De Souza, Marcus V. N.,De Oliveira, Marcone A. L.

, p. 887 - 898 (2015/05/20)

A methodology for the simultaneous determination of nelfinavir mesylate and the impurities 3-hydroxy-2-methylbenzoic acid and (2R,3R)-4-((3S,4aS,8aS)-3-(tert-butylcarbamoyl) octahydroisoquinolin-2(1H)-yl)-3-hydroxy-1-(phenylthio)butan-2-aminium benzoate by micellar electrokinetic chromatography, with an analysis time of 25 min, was proposed. An electrolyte composed of sodium tetraborate buffer (pH 9.24; 25 mmol L-1), sodium dodecyl sulphate (9 mmol L-1) and methanol (10percent, v/v) was optimized using a mixed-level factorial design, with direct detection at 200 nm. After evaluating some figures of merit, such as selectivity, linearity, precision, limit of detection, limit of quantification, accuracy and robustness (using Youden's test), the method was successfully applied to the analysis of nelfinavir mesylate and its impurities in a pharmaceutical formulation. The optimized methodology is demonstrated to be useful in the determination of these analytes in a synthesis monitoring process, in raw materials and in pharmaceutical formulations, while offering low solvent consumption, requiring a small sample and using non-specific columns as advantages.

A synthesis of the HIV-protease inhibitor nelfinavir from D-tartaric acid

Albizati, Kim F.,Babu, Srinivasan,Birchler, Angela,Busse, Juliette K.,Fugett, Michelle,Grubbs, Alan,Haddach, Aubrey,Pagan, Miguel,Potts, Barbara,Remarchuk, Travis,Rieger, Dale,Rodriguez, Rick,Shanley, Jim,Szendroi, Robert,Tibbetts, Tony,Whitten, Kathleen,Borer, Bennett C.

, p. 6481 - 6485 (2007/10/03)

This letter describes a new synthesis of the HIV-protease inhibitor nelfinavir. The synthesis features a selective opening of a D-tartaric acid-derived cyclic sulfate with nitrogen nucleophiles.

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