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1003924-50-2

α-(diethoxyphosphoryl)methyl 5-(1-phenyl)-1H-tetrazolyl sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1003924-50-2 Structure

  • Basic information

    1. Product Name: α-(diethoxyphosphoryl)methyl 5-(1-phenyl)-1H-tetrazolyl sulfide
    2. Synonyms: α-(diethoxyphosphoryl)methyl 5-(1-phenyl)-1H-tetrazolyl sulfide
    3. CAS NO:1003924-50-2
    4. Molecular Formula:
    5. Molecular Weight: 328.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1003924-50-2.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: α-(diethoxyphosphoryl)methyl 5-(1-phenyl)-1H-tetrazolyl sulfide(CAS DataBase Reference)
    10. NIST Chemistry Reference: α-(diethoxyphosphoryl)methyl 5-(1-phenyl)-1H-tetrazolyl sulfide(1003924-50-2)
    11. EPA Substance Registry System: α-(diethoxyphosphoryl)methyl 5-(1-phenyl)-1H-tetrazolyl sulfide(1003924-50-2)

  • 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: 1003924-50-2(Hazardous Substances Data)

1003924-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1003924-50-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,9,2 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1003924-50:
(9*1)+(8*0)+(7*0)+(6*3)+(5*9)+(4*2)+(3*4)+(2*5)+(1*0)=102
102 % 10 = 2
So 1003924-50-2 is a valid CAS Registry Number.

1003924-50-2Relevant articles and documents

Enantioselective synthesis of chiral sulfones by Rh-catalyzed asymmetric addition of boronic acids to α,β-unsaturated 2-pyridyl sulfones

Mauleon, Pablo,Alonso, Ines,Rivero, Marta Rodriguez,Carretero, Juan C.

, p. 9924 - 9935 (2007)

(Chemical Equation Presented) A general and efficient method for the rhodium-catalyzed enantioselective catalytic conjugate addition of organoboronic acids to α,β-unsaturated sulfones is described. The success of the process relies on the use of α,β-unsat

ISOTHIOCYANATE COMPOUND AND APPLICATION THEREOF

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Paragraph 0086; 0087, (2018/02/28)

The present invention provides an isothiocyanate compound and its application. The compound is an aryl-substituted isothiocyanate compound that has a structure of the general formula I. The isothiocyanate compound of the present invention has very good solubility in water, far better inhibitory activity for XPO1 protein than other non-aryl substituted congeneric compounds, little side effects, and good biological safety and bioavailability, and is quite suitable for clinical application. Therefore, the isothiocyanate compound would have tremendous potential market space and economic benefits.

Thermolyses of α-phosphorylmethyl tetrazolyl sulfoxides in the presence of 2,3-dimethyl-1,3-butadiene and their reactions with several amines

Morita, Hiroyuki,Tashiro, Shintaro,Takeda, Masahiro,Fujimori, Ken,Yamada, Nobuhiko,Chanmiya Sheikh,Kawaguchi, Hiroyuki

, p. 3589 - 3595 (2008/09/20)

We have synthesized α-(phosphoryl)methyl tetrazolyl sulfoxides and examined the reactivities in the thermolyses and in the presence of several amines, such as aniline, benzylamine, piperidine, pyrrolidine, and morpholine. Thermolyses of the derivatives in the presence of 2,3-dimethyl-1,3-butadiene afforded 2-phosphoryl substituted 4,5-dimethyl-3,6-dihydro-2H-thiopyran S-oxide. In addition, novel phosphinecarbothioamides were obtained in the reaction of the derivatives with amines.

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