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1038467-15-0

C17H21N3O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1038467-15-0 Structure

  • Basic information

    1. Product Name: C17H21N3O3S
    2. Synonyms:
    3. CAS NO:1038467-15-0
    4. Molecular Formula:
    5. Molecular Weight: 347.438
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1038467-15-0.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: C17H21N3O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H21N3O3S(1038467-15-0)
    11. EPA Substance Registry System: C17H21N3O3S(1038467-15-0)

  • 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: 1038467-15-0(Hazardous Substances Data)

1038467-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1038467-15-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,8,4,6 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1038467-15:
(9*1)+(8*0)+(7*3)+(6*8)+(5*4)+(4*6)+(3*7)+(2*1)+(1*5)=150
150 % 10 = 0
So 1038467-15-0 is a valid CAS Registry Number.

1038467-15-0Downstream Products

1038467-15-0Relevant articles and documents

Taurine isothiocyanate: a versatile intermediate for the preparation of ureas, thioureas, and guanidines. Taurine-derived cyclodextrins

Márquez, José M.,López, óscar,Maya, Inés,Fuentes, José,Fernández-Bola?os, José G.

, p. 3912 - 3915 (2008)

A versatile and expeditious synthesis of taurine-derived thioureas, ureas, and guanidines using taurine isothiocyanate as the key intermediate is reported. Thioureas were obtained by a one-pot two-step procedure starting from taurine by the isothiocyanation reaction with thiophosgene in aqueous THF, followed by coupling with aliphatic and aromatic amines. Desulfurization of thiourea derivatives with yellow mercury(II) oxide gave access to either taurine-containing ureas or guanidines in a one-pot three-step fashion. This methodology was successfully applied to the preparation of a cyclodextrin-derived thiourea and guanidine with a taurine residue in their structures.

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